Highly validated and characterized monoclonal/polyclonal
antibodies and recombinant
proteins
The majority of AAA Biotech’s antibodies are highly validated and can be use in multiple
applications such as ELISA, FC,
ICC, IF, IHC, IP, WB, etc. We have antibodies available for rare species, in multiple conjugated
forms or recombinant
antibodies.
As for our high quality proteins, the majority have 90% purity, detected by SDS-PAGE while some are
available in
different tags such as Flag, GST, His, MBP, etc. We also carry high quality native and biologically
active proteins.
AAA Biotech is constantly working to expand our capacity to provide recombinant proteins and
antibodies to most
target proteins.
SELECT `p`.*, `pd`.*, IFNULL(pdns.ncbi_summary, "N/A") as ncbi_summary_pdns, IFNULL(pdns.sp_comments, "N/A") as sp_comments_pdns, IFNULL(pdns.ncbi_research_articles, "N/A") as ncbi_research_articles_pdns, IFNULL(pe.products_description_extra, "N/A") as products_description_extra
FROM (`products`, `products` as `p`)
LEFT OUTER JOIN `products_description` as `pd` ON `p`.`products_id` = `pd`.`products_id`
LEFT OUTER JOIN `products_description_ncbi_sp` as `pdns` ON `p`.`products_id` = `pdns`.`products_id`
LEFT OUTER JOIN `products_extra` as `pe` ON `p`.`products_id` = `pe`.`products_id`
WHERE `p`.`products_id` = '28079'
AND `pd`.`language_id` = 1
LIMIT 1
Query
Database
3.71 ms
select p.*, pd.*,
ifnull(pdns.ncbi_summary, 'N/A') as ncbi_summary_pdns,
ifnull(pdns.sp_comments, 'N/A') as sp_comments_pdns,
ifnull(pdns.ncbi_research_articles, 'N/A') as ncbi_research_articles_pdns,
ifnull(pe.products_description_extra, 'N/A') as products_description_extra
from products p
LEFT OUTER JOIN products_description pd on p.products_id = pd.products_id
LEFT OUTER JOIN products_description_ncbi_sp pdns on p.products_id = pdns.products_id
LEFT OUTER JOIN products_extra pe on p.products_id = pe.products_id
where p.products_id = '28079' and pd.language_id = 1
Query
Database
1.39 ms
SELECT `options_values_price` as `price`, `products_options_values_name` as `package`
FROM `products_attributes`
JOIN `products_options_values` ON `products_options_values`.`products_options_values_id` = `products_attributes`.`options_values_id`
WHERE `products_attributes`.`products_id` = '28079'
Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
2.55 ms
SELECT `p`.*, `pd`.*, IFNULL(pdns.ncbi_summary, "N/A") as ncbi_summary_pdns, IFNULL(pdns.sp_comments, "N/A") as sp_comments_pdns, IFNULL(pdns.ncbi_research_articles, "N/A") as ncbi_research_articles_pdns, IFNULL(pe.products_description_extra, "N/A") as products_description_extra
FROM (`products`, `products` as `p`)
LEFT OUTER JOIN `products_description` as `pd` ON `p`.`products_id` = `pd`.`products_id`
LEFT OUTER JOIN `products_description_ncbi_sp` as `pdns` ON `p`.`products_id` = `pdns`.`products_id`
LEFT OUTER JOIN `products_extra` as `pe` ON `p`.`products_id` = `pe`.`products_id`
WHERE `p`.`products_id` = '28079'
AND `pd`.`language_id` = 1
LIMIT 1
select p.*, pd.*,
ifnull(pdns.ncbi_summary, 'N/A') as ncbi_summary_pdns,
ifnull(pdns.sp_comments, 'N/A') as sp_comments_pdns,
ifnull(pdns.ncbi_research_articles, 'N/A') as ncbi_research_articles_pdns,
ifnull(pe.products_description_extra, 'N/A') as products_description_extra
from products p
LEFT OUTER JOIN products_description pd on p.products_id = pd.products_id
LEFT OUTER JOIN products_description_ncbi_sp pdns on p.products_id = pdns.products_id
LEFT OUTER JOIN products_extra pe on p.products_id = pe.products_id
where p.products_id = '28079' and pd.language_id = 1
SELECT `options_values_price` as `price`, `products_options_values_name` as `package`
FROM `products_attributes`
JOIN `products_options_values` ON `products_options_values`.`products_options_values_id` = `products_attributes`.`options_values_id`
WHERE `products_attributes`.`products_id` = '28079'
⇄⧉testing_protocols => string (1115) "IHC (Immunohistchemistry)||Immunohistochemistry of paraffin-embedded mouse c...
$value['testing_protocols']
IHC (Immunohistchemistry)||Immunohistochemistry of paraffin-embedded mouse cerebellum using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC6.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded mouse brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat lung using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC2.jpg!!WB (Western Blot)||Western blot analysis of extracts of various cell lines, using RARA antibody at 1:1000 dilution.<br>Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.<br>Lysates/proteins: 25ug per lane.<br>Blocking buffer: 3% nonfat dry milk in TBST.<br>Detection: ECL Basic Kit.<br>Exposure time: 10s.||AAA28079_WB.jpg
⇄⧉products_description => string (1227) "Retinoids (vitamin A and its active retinoic acid derivatives) are non-stero...
$value['products_description']
Retinoids (vitamin A and its active retinoic acid derivatives) are non-steroid hormones that regulate cell proliferation, differentiation and apoptosis. Retinoic acid receptors (RARalpha, -beta and -gamma) and retinoid X receptors (RXRalpha, -beta and -gamma) are nuclear receptors that function as RAR-RXR heterodimers or RXR homodimers (1-2). In response to retinoid binding, these dimers control gene expression by binding to specific retinoic acid response elements, by recruiting cofactors and the transcriptional machinery, and by indirectly regulating chromatin structure. Finally, ligand binding and phosphorylation of RARalpha by JNK at Thr181, Ser445 and Ser461 controls the stability of RAR-RXR through the ubiquitin-proteasome pathway (3-4). At least four distinct genetic lesions affect RARalpha and result in acute promyelocytic leukemia (APL). The t(15;17) translocation that results in the PML-RARalpha fusion protein is responsible for more than 99% of APL cases, and the fusion protein inhibits PML-dependent apoptotic pathways in a dominant negative fashion. In addition PML-RARalpha inhibits transcription of retinoic acid target genes by recruiting co-repressors, attenuating myeloid differentiation (5-6).
⇄⧉testing_protocols => string (1115) "IHC (Immunohistchemistry)||Immunohistochemistry of paraffin-embedded mouse c...
$value->a['testing_protocols']
IHC (Immunohistchemistry)||Immunohistochemistry of paraffin-embedded mouse cerebellum using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC6.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded mouse brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat lung using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC2.jpg!!WB (Western Blot)||Western blot analysis of extracts of various cell lines, using RARA antibody at 1:1000 dilution.<br>Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.<br>Lysates/proteins: 25ug per lane.<br>Blocking buffer: 3% nonfat dry milk in TBST.<br>Detection: ECL Basic Kit.<br>Exposure time: 10s.||AAA28079_WB.jpg
⇄⧉products_description => string (1227) "Retinoids (vitamin A and its active retinoic acid derivatives) are non-stero...
$value->a['products_description']
Retinoids (vitamin A and its active retinoic acid derivatives) are non-steroid hormones that regulate cell proliferation, differentiation and apoptosis. Retinoic acid receptors (RARalpha, -beta and -gamma) and retinoid X receptors (RXRalpha, -beta and -gamma) are nuclear receptors that function as RAR-RXR heterodimers or RXR homodimers (1-2). In response to retinoid binding, these dimers control gene expression by binding to specific retinoic acid response elements, by recruiting cofactors and the transcriptional machinery, and by indirectly regulating chromatin structure. Finally, ligand binding and phosphorylation of RARalpha by JNK at Thr181, Ser445 and Ser461 controls the stability of RAR-RXR through the ubiquitin-proteasome pathway (3-4). At least four distinct genetic lesions affect RARalpha and result in acute promyelocytic leukemia (APL). The t(15;17) translocation that results in the PML-RARalpha fusion protein is responsible for more than 99% of APL cases, and the fusion protein inhibits PML-dependent apoptotic pathways in a dominant negative fashion. In addition PML-RARalpha inhibits transcription of retinoic acid target genes by recruiting co-repressors, attenuating myeloid differentiation (5-6).
⇄⧉testing_protocols => string (1115) "IHC (Immunohistchemistry)||Immunohistochemistry of paraffin-embedded mouse c...
$value->d['testing_protocols']
IHC (Immunohistchemistry)||Immunohistochemistry of paraffin-embedded mouse cerebellum using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC6.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded mouse brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat lung using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded rat brain using RARA antibody at dilution of 1:100 (40x lens).||AAA28079_IHC2.jpg!!WB (Western Blot)||Western blot analysis of extracts of various cell lines, using RARA antibody at 1:1000 dilution.<br>Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.<br>Lysates/proteins: 25ug per lane.<br>Blocking buffer: 3% nonfat dry milk in TBST.<br>Detection: ECL Basic Kit.<br>Exposure time: 10s.||AAA28079_WB.jpg
⇄⧉products_description => string (1227) "Retinoids (vitamin A and its active retinoic acid derivatives) are non-stero...
$value->d['products_description']
Retinoids (vitamin A and its active retinoic acid derivatives) are non-steroid hormones that regulate cell proliferation, differentiation and apoptosis. Retinoic acid receptors (RARalpha, -beta and -gamma) and retinoid X receptors (RXRalpha, -beta and -gamma) are nuclear receptors that function as RAR-RXR heterodimers or RXR homodimers (1-2). In response to retinoid binding, these dimers control gene expression by binding to specific retinoic acid response elements, by recruiting cofactors and the transcriptional machinery, and by indirectly regulating chromatin structure. Finally, ligand binding and phosphorylation of RARalpha by JNK at Thr181, Ser445 and Ser461 controls the stability of RAR-RXR through the ubiquitin-proteasome pathway (3-4). At least four distinct genetic lesions affect RARalpha and result in acute promyelocytic leukemia (APL). The t(15;17) translocation that results in the PML-RARalpha fusion protein is responsible for more than 99% of APL cases, and the fusion protein inhibits PML-dependent apoptotic pathways in a dominant negative fashion. In addition PML-RARalpha inhibits transcription of retinoic acid target genes by recruiting co-repressors, attenuating myeloid differentiation (5-6).
⇄⧉specificity => string (175) "This assay has high sensitivity and excellent specificity for detection of R...
$value[0]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of Rat SYP. No significant cross-reactivity or interference between Rat SYP and analogues was observed.
⇄purity => string (3) "N/A"
$value[0]['_source']['purity']
⇄form => string (3) "N/A"
$value[0]['_source']['form']
⇄concentration => string (3) "N/A"
$value[0]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[0]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term1 => string (132) "Samples||Tissue homogenates, serum and plasma!!Assay Type||Sandwich!!Detecti...
$value[0]['_source']['etc_term1']
Samples||Tissue homogenates, serum and plasma!!Assay Type||Sandwich!!Detection Range||0.625 ng/ml-40 ng/ml!!Sensitivity||0.156 ng/ml
⇄⧉etc_term2 => string (391) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[0]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV% is less than 8%<br>Three samples of known concentration were tested twenty times on one plate to assess.<br>Inter-assay Precision (Precision between assays): CV% is less than 10%<br>Three samples of known concentration were tested in twenty assays to assess.!!Detection Wavelength||450 nm!!Sample Volume||50-100ul
⇄⧉products_name_syn => string (92) "Rat Synaptophysin (Syp) ELISA kit; MRXSYP; major synaptic vesicle protein P3...
$value[0]['_source']['products_name_syn']
Rat Synaptophysin (Syp) ELISA kit; MRXSYP; major synaptic vesicle protein P38; synaptophysin
⇄products_gene_name => string (3) "SYP"
$value[0]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[0]['_source']['products_gene_name_syn']
⇄⧉products_description => string (774) "<b>Principle of the Assay: </b>This assay employs the quantitative sandwich ...
$value[0]['_source']['products_description']
<b>Principle of the Assay: </b>This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for synaptophysin has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any synaptophysin present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for synaptophysin is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of synaptophysin bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
$value[0]['_source']['products_references']
⇄⧉products_related_diseases => string (230) "Nervous System Diseases||58!!Brain Diseases||46!!Disease Models, Animal||31!...
⇄⧉search_terms => string (671) "aaa15342 rat this assay has high sensitivity and excellent specificity for d...
$value[0]['_source']['search_terms']
aaa15342 rat this assay has high sensitivity and excellent specificity for detection of syp no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15342_td elisa kit synaptophysin mrxsyp major synaptic vesicle protein p38 syp1 33,311 da syph_rat 6981622 np_036796.1 p07825 nm_012664.2 q499r3 samples tissue homogenates serum plasma type sandwich range 0.625 ng ml 40 0.156 intra precision within an cv is less than 8 three known concentration were tested twenty times on one plate to assess inter assays 10 in wavelength 450 nm sample volume 50 100ul ml40 than8 assays10 wavelength450 volume50
⇄⧉specificity => string (162) "This SYP antibody is generated from rabbits immunized with a KLH conjugated ...
$value[1]['_source']['specificity']
This SYP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 225-253 amino acids from the C-terminal region of human SYP.
⇄⧉form => string (172) "Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. ...
$value[1]['_source']['form']
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
FCM (Flow Cytometry)||SYP Antibody (C-term) flow cytometric analysis of Neuro-2a cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.||AAA28723_FCM6.jpg!!IF (Immunofluorescence)||Confocal immunofluorescent analysis of SYP Antibody (C-term) with mouse brain tissue followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green).DAPI was used to stain the cell nuclear (blue).||AAA28723_IF5.jpg!!IF (Immunofluorescence)||Confocal immunofluorescent analysis of SYP Antibody (C-term) with human brain tissue followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green).DAPI was used to stain the cell nuclear (blue).||AAA28723_IF4.jpg!!IHC (Immunohistochemistry)||SYP Antibody (C-term) immunohistochemistry analysis in formalin fixed and paraffin embedded mouse hippocampus tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.This data demonstrates the use of SYP Antibody (C-term) for immunohistochemistry. Clinical relevance has not been evaluated.||AAA28723_IHC3.jpg!!IHC (Immunohistochemistry)||SYP Antibody (C-term) immunohistochemistry analysis in formalin fixed and paraffin embedded human brain tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.This data demonstrates the use of SYP Antibody (C-term) for immunohistochemistry. Clinical relevance has not been evaluated.||AAA28723_IHC2.jpg!!WB (Western Blot)||SYP Antibody (C-term) western blot analysis in mouse brain and cerebellum tissue lysates (35ug/lane).This demonstrates the SYP antibody detected the SYP protein (arrow).||AAA28723_WB.jpg
⇄products_name_syn => string (54) "Synaptophysin; Major synaptic vesicle protein p38; SYP"
$value[1]['_source']['products_name_syn']
⇄products_gene_name => string (3) "SYP"
$value[1]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[1]['_source']['products_gene_name_syn']
⇄⧉products_description => string (127) "Synaptophysin (p38) is an integral membrane protein of small synaptic vesicl...
$value[1]['_source']['products_description']
Synaptophysin (p38) is an integral membrane protein of small synaptic vesicles in brain and endocrine cells.[supplied by OMIM].
⇄⧉products_references => string (290) "Ishida, M., et al. Oncol. Rep. 22(4):733-737(2009) Sterlacci, W., et al. Vir...
$value[1]['_source']['products_references']
Ishida, M., et al. Oncol. Rep. 22(4):733-737(2009) Sterlacci, W., et al. Virchows Arch. 455(2):125-132(2009) Head, E., et al. Neurobiol. Aging 30(7):1125-1134(2009) Gulubova, M., et al. J. Gastroenterol. Hepatol. 23(10):1574-1585(2008) Glantz, L.A., et al. Neuroscience 149(3):582-591(2007)
⇄⧉products_related_diseases => string (251) "Nervous System Diseases||85!!Brain Diseases||69!!Disease Models, Animal||46!...
⇄⧉search_terms => string (1167) "aaa28723 rabbit human mouse predicted reactivity rat polyclonal ig peptide a...
$value[1]['_source']['search_terms']
aaa28723 rabbit human mouse predicted reactivity rat polyclonal ig peptide affinity purified antibody pab supplied in pbs with 0.09 w v sodium azide this is through a protein column followed by purification syp generated from rabbits immunized klh conjugated synthetic between 225 253 amino acids the c terminal region of elisa eia flow cytometry fc facs immunofluorescence if immunohistochemistry ihc western blot wb wb~~1:2000 ihc~~1:1000 if~~1:100 fc~~1:50 term analysis brain and cerebellum tissue lysates 35ug lane demonstrates detected arrow aaa28723_wb formalin fixed paraffin embedded peroxidase conjugation secondary dab staining.this data use for clinical relevance has not been evaluated aaa28723_ihc2 hippocampus aaa28723_ihc3 confocal immunofluorescent alexa fluor 488 goat anti lgg green dapi was used to stain cell nuclear blue aaa28723_if4 aaa28723_if5 cytometric neuro 2a cells right histogram compared negative control left fitc antibodies were aaa28723_fc6 synaptophysin major synaptic vesicle p38 mrx96 mrxsyp 33845 syph_human 27764867 np_003170.1 p08247 nm_003179.2 q6p2f7 b2r7l6 b7z359 300802 neuroscience antigen type source between225 fluor488
ICC (Immunocytochemistry)||ICC staining Synaptophysin in PC-12 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA30051_ICC6.jpg!!ICC (Immunocytochemistry)||ICC staining Synaptophysin in N2A cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA30051_ICC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded mouse pancreas tissue using anti-Synaptophysin antibody. Counter stained with hematoxylin.||AAA30051_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-Synaptophysin antibody. Counter stained with hematoxylin.||AAA30051_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human pancreas tissue using anti-Synaptophysin antibody. Counter stained with hematoxylin.||AAA30051_IHC2.jpg!!WB (Western Blot)||Western blot analysis of Synaptophysin on different lysates using anti-Synaptophysin at 1/500 dilution. Positive control�� <br/>Lane 1: Human brain <br/>Lane 2: PC-12||AAA30051_WB.jpg
Major synaptic vesicle protein p38 antibody; MRX96 antibody; MRXSYP antibody; Syn p38 antibody; Synaptophysin antibody; Syp antibody; SYPH antibody; SYPH_HUMAN antibody; SypI antibody
⇄products_gene_name => string (3) "N/A"
$value[2]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[2]['_source']['products_gene_name_syn']
⇄⧉products_description => string (1076) "Synaptic vesicles participate in a cycle of fusion with the plasma membrane ...
$value[2]['_source']['products_description']
Synaptic vesicles participate in a cycle of fusion with the plasma membrane and reformation by endocytosis. Synaptic vesicle protein synaptophysin (SYP) is targeted to early endosomes in transfected fibroblasts and in neuroendocrine cells. SYP is an N-glycosylated intergral membrane protein found in neurons and endocrine cells that associates into hexamers to form a large conductance channel. SYP contains four transmembrane domains and may function as a gap juction-like channel. Membrane cholesterol specfically interacts with SYP to play a role in vesicle formation. Synaptobrevin (VAMP) also binds to SYP and the resultant complex is upregulated during neuronal development, but is absent in exocytosis fusion complex. Thus, the synaptophysin-synaptobrevin complex is not essential for exocytosis, but rather provides a pool of synaptobrevin for exocytosis. In addition, the tail domain of brain Myosin V also forms a stable complex with synaptobrevin II and SYP, and this complex is disassembled upon the depolarization-induced entry of Ca2+ into intact nerve endings.
⇄products_references => string (3) "N/A"
$value[2]['_source']['products_references']
⇄⧉products_related_diseases => string (241) "Nervous System Diseases||44!!Brain Diseases||34!!Disease Models, Animal||20!...
⇄⧉search_terms => UTF-8 string (916) "aaa30051 rabbit human mouse rat monoclonal sj26 85 proa affinity purified 1*...
$value[2]['_source']['search_terms']
aaa30051 rabbit human mouse rat monoclonal sj26 85 proa affinity purified 1*tbs ph7.4 1 bsa 40 glycerol preservative 0.05 sodium azide western blot wb immunocytochemistry icc immunofluorescence if immunohistochemistry ihc 1:1000 5000 1:50 1:200 analysis of synaptophysin on different lysates using anti at 500 dilution positive control�� < br > lane brain 2 pc 12 aaa30051_wb immunohistochemical paraffin embedded pancreas tissue antibody counter stained with hematoxylin aaa30051_ihc2 aaa30051_ihc3 aaa30051_ihc4 staining in n2a cells red the nuclear stain is dapi blue were fixed paraformaldehyde permeabilised 0.25 triton x100 pbs aaa30051_icc5 aaa30051_icc6 major synaptic vesicle protein p38 mrx96 mrxsyp syn syp syph syph_human sypi 33,845 da 27764867 np_003170.1 p08247 nm_003179.2 q6p2f7 b2r7l6 300802 total ab type recombinant immunogen conjugation unconjugated sj2685 ph7.41 bsa40 at500 brain2 pc12
⇄⧉specificity => string (718) "Phospho-LRRK2 (Ser935) Antibody detects endogenous levels of LRRK2 only when...
$value[3]['_source']['specificity']
Phospho-LRRK2 (Ser935) Antibody detects endogenous levels of LRRK2 only when phosphorylated at Ser935.<br>Tissue Specificity: Expressed in pyramidal neurons in all cortical laminae of the visual cortex, in neurons of the substantia nigra pars compacta and caudate putamen (at protein level). Expressed in neutrophils (at protein level). Expressed in the brain. Expressed throughout the adult brain, but at a lower level than in heart and liver. Also expressed in placenta, lung, skeletal muscle, kidney and pancreas. In the brain, expressed in the cerebellum, cerebral cortex, medulla, spinal cord occipital pole, frontal lobe, temporal lobe and putamen. Expression is particularly high in brain dopaminoceptive areas.
⇄⧉purity => string (158) "The antibody is from purified rabbit serum by affinity purification via sequ...
$value[3]['_source']['purity']
The antibody is from purified rabbit serum by affinity purification via sequential chromatography on phospho-peptide and non-phospho-peptide affinity columns.
⇄⧉testing_protocols => string (1847) "Application Data||At 25 degree C. Samples were then incubated with primary A...
$value[3]['_source']['testing_protocols']
Application Data||At 25 degree C. Samples were then incubated with primary Ab(At 37 degree C. An AlexaFluor594 conjugated goat anti-rabbit IgG(H+L) Ab(Red) and an AlexaFluor488 conjugated goat anti-mouse IgG(H+L) Ab(Green) were used as the secondary antibody.<br>The nuclear counter stain is DAPI (blue).||AAA31287_APP6.jpg!!IHC (Immunohistochemistry)||At 1/100 staining Mouse heart tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the primary antibody at 4 degree C overnight. An HRP conjugated anti-Rabbit antibody was used as the secondary antibody.||AAA31287_IHC5.jpg!!IHC (Immunohistochemistry)||At 1/100 staining Mouse skin tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the primary antibody at 4 degree C overnight. An HRP conjugated anti-Rabbit antibody was used as the secondary antibody.||AAA31287_IHC4.jpg!!IHC (Immunohistochemistry)||At 1/100 staining Rat skin tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the primary antibody at 4 degree C overnight. An HRP conjugated anti-Rabbit antibody was used as the secondary antibody.||AAA31287_IHC3.jpg!!WB (Western Blot)||Western blot analysis of extracts from P19 cells(LPS treatment), using Phospho-LRRK2 (Ser935) Antibody. The lane on the left was treated with blocking peptide.||AAA31287_WB2.jpg!!WB (Western Blot)||Western blot analysis of extracts from K562 cells(serum starvation treatment), using Phospho-LRRK2 (Ser935) Antibody. The lane on the left was treated with blocking peptide.||AAA31287_WB.jpg
⇄⧉etc_term1 => string (151) "Immunogen||A synthesized peptide derived from human LRRK2 around the phospho...
$value[3]['_source']['etc_term1']
Immunogen||A synthesized peptide derived from human LRRK2 around the phosphorylation site of Ser935.!!Conjugation||Unconjugated!!Fragment||Fab fragment
⇄⧉etc_term2 => string (1730) "Post Translational Modifications||Autophosphorylated. Phosphorylation of Ser...
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Post Translational Modifications||Autophosphorylated. Phosphorylation of Ser-910 and either Ser-935 or Ser-1444 facilitates interaction with YWHAG. Phosphorylation of Ser-910 and/or Ser-935 facilitates interaction with SFN.!!Subunit Structure||Homodimer. Interacts with PRKN, PRDX3, and TPCN2. Interacts with VPS35 and RAB29. Interacts (via ROC domain) with SEC16A. Interacts with APP; interaction promotes phosphorylation of 'Thr-743' of APP. Interacts with MAPT. Interacts with RAB8A, RAB10, and RAB12. Interacts with YWHAG; this interaction is dependent on phosphorylation of Ser-910 and either Ser-935 or Ser-1444. Interacts with SFN; this interaction is dependent on phosphorylation of Ser-910 and/or Ser-935.!!Similarity||The seven-bladed WD repeat region is critical for synaptic vesicle trafficking and mediates interaction with multiple vesicle-associated presynaptic proteins (PubMed:24687852). It also mediates homodimerization and regulates kinase activity (PubMed:30635421).The Roc domain mediates homodimerization and regulates kinase activity.Belongs to the protein kinase superfamily. TKL Ser/Thr protein kinase family.!!Subcellular Location||Cytoplasmic vesicle. Perikaryon. Golgi apparatus membrane>Peripheral membrane protein. Cell projection>Axon. Cell projection>Dendrite. Endoplasmic reticulum membrane>Peripheral membrane protein. Cytoplasmic vesicle>Secretory vesicle>Synaptic vesicle membrane. Endosome. Lysosome. Mitochondrion outer membrane>Peripheral membrane protein.<br>Note: Colocalized with RAB29 along tubular structures emerging from Golgi apparatus (PubMed:23395371). Localizes to endoplasmic reticulum exit sites (ERES), also known as transitional endoplasmic reticulum (tER) (PubMed:25201882).
⇄⧉products_description => string (1939) "Serine/threonine-protein kinase which phosphorylates a broad range of protei...
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Serine/threonine-protein kinase which phosphorylates a broad range of proteins involved in multiple processes such as neuronal plasticity, autophagy, and vesicle trafficking. Is a key regulator of RAB GTPases by regulating the GTP/GDP exchange and interaction partners of RABs through phosphorylation. Phosphorylates RAB3A, RAB3B, RAB3C, RAB3D, RAB5A, RAB5B, RAB5C, RAB8A, RAB8B, RAB10, RAB12, RAB35, and RAB43. Regulates the RAB3IP-catalyzed GDP/GTP exchange for RAB8A through the phosphorylation of 'Thr-72' on RAB8A. Inhibits the interaction between RAB8A and GDI1 and/or GDI2 by phosphorylating 'Thr-72' on RAB8A. Regulates primary ciliogenesis through phosphorylation of RAB8A and RAB10, which promotes SHH signaling in the brain. Together with RAB29, plays a role in the retrograde trafficking pathway for recycling proteins, such as mannose-6-phosphate receptor (M6PR), between lysosomes and the Golgi apparatus in a retromer-dependent manner. Regulates neuronal process morphology in the intact central nervous system (CNS). Plays a role in synaptic vesicle trafficking. Plays an important role in recruiting SEC16A to endoplasmic reticulum exit sites (ERES) and in regulating ER to Golgi vesicle-mediated transport and ERES organization. Positively regulates autophagy through a calcium-dependent activation of the CaMKK/AMPK signaling pathway. The process involves activation of nicotinic acid adenine dinucleotide phosphate (NAADP) receptors, increase in lysosomal pH, and calcium release from lysosomes. Phosphorylates PRDX3. By phosphorylating APP on 'Thr-743', which promotes the production and the nuclear translocation of the APP intracellular domain (AICD), regulates dopaminergic neuron apoptosis. Independent of its kinase activity, inhibits the proteosomal degradation of MAPT, thus promoting MAPT oligomerization and secretion. In addition, has GTPase activity via its Roc domain which regulates LRRK2 kinase activity.
⇄products_references => string (3) "N/A"
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⇄⧉products_related_diseases => string (266) "Nervous System Diseases||804!!Movement Disorders||780!!Parkinson Disease||77...
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aaa31287 rabbit human mouse rat polyclonal igg the antibody is from purified serum by affinity purification via sequential chromatography on phospho peptide and non columns liquid in phosphate buffered saline ph7.4 150mm nacl 0.02 sodium azide 50 glycerol lrrk2 ser935 detects endogenous levels of only when phosphorylated at tissue specificity expressed pyramidal neurons all cortical laminae visual cortex substantia nigra pars compacta caudate putamen protein level neutrophils brain throughout adult but a lower than heart liver also placenta lung skeletal muscle kidney pancreas cerebellum cerebral medulla spinal cord occipital pole frontal lobe temporal expression particularly high dopaminoceptive areas western blot wb immunohistochemistry ihc immunofluorescence if immunocytochemistry icc elisa eia 1:50 1:200 1:100 1:500 1:2000 1:20,000 1:40,000 analysis extracts k562 cells starvation treatment using lane left was treated with blocking aaa31287_wb p19 lps aaa31287_wb2 1 100 staining skin p sample formaldehyde fixed heat mediated antigen retrieval step citrate buffer performed then blocked incubated primary 4 degree c overnight an hrp conjugated anti used as secondary aaa31287_ihc3 aaa31287_ihc4 aaa31287_ihc5 testing data 25 samples were ab 37 alexafluor594 goat h+l red alexafluor488 green nuclear counter stain dapi blue aaa31287_td6 augmented rheumatoid arthritis 17 aura17 dardarin leucine rich repeat kinase 2 serine threonine lrrk lrrk2_human park 8 park8 ripk7 roco roco2 2527 171846278 np_940980.3 q5s007 nm_198578.3 q6zs50 q8ncx9 a6nju2 168600 immunogen synthesized derived around phosphorylation site conjugation unconjugated fragment fab post translational modifications autophosphorylated ser 910 either 935 or 1444 facilitates interaction ywhag sfn subunit structure homodimer interacts prkn prdx3 tpcn2 vps35 rab29 roc domain sec16a app promotes 'thr 743' mapt rab8a rab10 rab12 this dependent similarity seven bladed wd region critical for synaptic vesicle trafficking mediates multiple associated presynaptic proteins pubmed:24687852 it homodimerization regulates activity pubmed:30635421 activity.belongs to superfamily tkl thr family subcellular location cytoplasmic perikaryon golgi apparatus membrane>peripheral membrane cell projection>axon projection>dendrite endoplasmic reticulum vesicle>secretory vesicle>synaptic endosome lysosome mitochondrion outer note colocalized along tubular structures emerging pubmed:23395371 localizes exit sites eres known transitional ter pubmed:25201882 azide50 aaa31287_wb21 primary4 data25 ab37 arthritis17 kinase2 ser910 either935
⇄⧉etc_term1 => string (174) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
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Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Competitive or Sandwich!!Detection Range||50-1000ng/mL!!Sensitivity||1.0ng/mL
⇄etc_term2 => string (3) "N/A"
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⇄products_name => string (52) "Phosphorylation P38 Mitogen activated Protein Kinase"
⇄⧉products_description => string (1495) "Intended Uses: This PMAPKP38 ELISA kit is a 1.5 hour solid-phase ELISA desig...
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Intended Uses: This PMAPKP38 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human PMAPKP38. This ELISA kit for research use only!<br><br>Principle of the Assay: PMAPKP38 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for PMAPKP38. Standards or samples are then added to the microtiter plate wells and PMAPKP38 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of PMAPKP38 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for PMAPKP38 are added to each well to "sandwich" the PMAPKP38 immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain PMAPKP38 and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The PMAPKP38 concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (332) "aaa16598 human typical testing data standard curve for reference only aaa165...
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aaa16598 human typical testing data standard curve for reference only aaa16598_sc elisa kit phosphorylation p38 mitogen activated protein kinase p p38mapk cell biology samples serum plasma culture supernatants body fluid and tissue homogenate assay type competitive or sandwich detection range 50 1000ng ml sensitivity 1.0ng range50
⇄⧉products_description => string (674) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
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Principle of the Assay: This experiment use double-sandwich elisa technique and the ELISA Kit provided is typical. The pre-coated antibody is human PLP monoclonal antibody and the detecting antibody is polyclonal antibody with biotin labeled. Samples and biotin labeling antibody are added into ELISA plate wells and washed out with PBS or TBS. Then Avidin-peroxidase conjugates are added to ELISA wells in order; Use TMB substrate for coloring after reactant thoroughly washed out by PBS or TBS. TMB turns into blue in peroxidase catalytic and finally turns into yellow under the action of acid. The color depth and the testing factors in samples are positively correlated.
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⇄⧉products_related_diseases => string (247) "Nervous System Diseases||190!!Pelizaeus-Merzbacher Disease||129!!Disease Mod...
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Nervous System Diseases||190!!Pelizaeus-Merzbacher Disease||129!!Disease Models, Animal||78!!Nerve Degeneration||20!!Spastic paraplegia 2, X-linked||17!!Inflammation||12!!Nervous System Malformations||11!!Drug Toxicity||10!!Atrophy||8!!Seizures||7
⇄products_categories => string (3) "N/A"
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⇄ncbi_full_name => string (36) "myelin proteolipid protein isoform 1"
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⇄ncbi_full_name_syn => string (21) "proteolipid protein 1"
⇄⧉search_terms => string (493) "aaa12940 human no cross reaction with other factors typical testing data sta...
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aaa12940 human no cross reaction with other factors typical testing data standard curve for reference only aaa12940_sc elisa kit myelin proteolipid protein plp isoform 1 plp1 pmd hld1 mmpl spg2 gpm6c dm20 lipophilin major 26,274 da mypr_human 192449447 np_001122306.1 p60201 nm_001128834.1 p04400 p06905 q502y1 q6fhz6 312920 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 10 ng ml 0.156 sensitivity up to 0.05 intra precision isoform1 range10
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
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This assay has high sensitivity and excellent specificity for detection of human HBeAg. No significant cross-reactivity or interference between human HBeAg and analogues was observed.
⇄purity => string (3) "N/A"
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⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
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Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (300) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
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Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<15%. Three positive samples were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<20%. Three positive samples were tested in twenty assays to assess.
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⇄products_name => string (34) "Hepatitis B Virus e Antigen, HBeAg"
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⇄products_name_oem => string (50) "Human Hepatitis B Virus e Antigen, HBeAg ELISA Kit"
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⇄⧉products_name_syn => string (82) "Human Hepatitis B e Antigen (HBeAg) ELISA Kit; Human Hepatitis B e Antigen (...
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Human Hepatitis B e Antigen (HBeAg) ELISA Kit; Human Hepatitis B e Antigen (HBeAg)
⇄products_gene_name => string (5) "HBeAg"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (526) "Principle of the Assay: This assay employs the qualitative sandwich enzyme i...
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Principle of the Assay: This assay employs the qualitative sandwich enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with HBeAb. Standards and samples are pipetted into the wells with a Horseradish Peroxidase (HRP) conjugated HBeAb. Following a wash to remove any unbound reagent, a substrate solution is added to the wells and color develops in proportion to the amount of HBeAg bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (507) "aaa15174 human this assay has high sensitivity and excellent specificity for...
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aaa15174 human this assay has high sensitivity and excellent specificity for detection of hbeag no significant cross reactivity or interference between analogues was observed elisa kit hepatitis b virus e antigen 24,643 da core major nucleocapsid protein hbcag prec c precore precore+core q15194_hbv 22530876 aam96930.1 q15194 q89499 samples serum plasma type qualitative sandwich intra precision within an cv <15 three known concentration were tested twenty times on one plate to assess inter assays <20 in
⇄⧉testing_protocols => string (1209) "IF (Immunofluorescence)||Immunofluorescence analysis of C6 cells using LRRK2...
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IF (Immunofluorescence)||Immunofluorescence analysis of C6 cells using LRRK2 Rabbit pAb at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.||AAA28347_IF6.jpg!!IF (Immunofluorescence)||Immunofluorescence analysis of C2C12 cells using LRRK2 Rabbit pAb at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.||AAA28347_IF5.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded Human placenta using LRRK2 Rabbit pAb at dilution of 1:100 (40x lens).||AAA28347_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded Rat brain using LRRK2 Rabbit pAb at dilution of 1:100 (40x lens).||AAA28347_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded Mouse kidney using LRRK2 Rabbit pAb at dilution of 1:100 (40x lens).||AAA28347_IHC2.jpg!!WB (Western Blot)||Western blot analysis of extracts of various cell lines, using LRRK2 Polyclonal Antibody at 1:1000 dilution.<br />Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.<br />Lysates/proteins: 25ug per lane.<br />Blocking buffer: 3% nonfat dry milk in TBST.<br />Detection: ECL Basic Kit (RM00020).<br />Exposure time: 3min.||AAA28347_WB.jpg
⇄⧉etc_term1 => string (535) "Immunogen||Recombinant fusion protein containing a sequence corresponding to...
⇄⧉products_description => string (444) "Background: This gene is a member of the leucine-rich repeat kinase family a...
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Background: This gene is a member of the leucine-rich repeat kinase family and encodes a protein with an ankryin repeat region, a leucine-rich repeat (LRR) domain, a kinase domain, a DFG-like motif, a RAS domain, a GTPase domain, a MLK-like domain, and a WD40 domain. The protein is present largely in the cytoplasm but also associates with the mitochondrial outer membrane. Mutations in this gene have been associated with Parkinson disease-8.
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⇄⧉products_related_diseases => string (266) "Nervous System Diseases||804!!Movement Disorders||780!!Parkinson Disease||77...
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of M...
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This assay has high sensitivity and excellent specificity for detection of MAP. No significant cross-reactivity or interference between MAP and analogues was observed.
⇄purity => string (3) "N/A"
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Store entire kit at 2-8C for short-term. For longer-term, please store the microplate & standard at -20C, while the remaining reagents can be stored at 2-8C
⇄⧉products_name_syn => string (114) "Inter-alpha-trypsin inhibitor heavy chain H4; ITI heavy chain H4; Inter-alph...
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Inter-alpha-trypsin inhibitor heavy chain H4; ITI heavy chain H4; Inter-alpha-inhibitor heavy chain 4; ITIH4; IHRP
⇄products_gene_name => string (3) "MAP"
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⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
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Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
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⇄⧉search_terms => string (466) "aaa27540 porcine this assay has high sensitivity and excellent specificity f...
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aaa27540 porcine this assay has high sensitivity and excellent specificity for detection of map no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa27540_sc elisa kit major acute phase protein inter alpha trypsin inhibitor heavy chain h4 iti 4 itih4 ihrp 205302 samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 0.156 10ng ml 0.094ng iti4
⇄⧉products_description => string (678) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
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Principle of the Assay: This experiment use double-sandwich elisa technique and the ELISA Kit provided is typical. The pre-coated antibody is Rabbit ICAM-1 monoclonal antibody and the detecting antibody is polyclonal antibody with biotin labeled. Samples and biotin labeling antibody are added into ELISA plate wells and washed out with PBS or TBS. Then Avidin-peroxidase conjugates are added to ELISA wells in order; Use TMB substrate for coloring after reactant thoroughly washed out by PBS or TBS. TMB turns into blue in peroxidase catalytic and finally turns into yellow under the action of acid. The color depth and the testing factors in samples are positively correlated.
⇄⧉search_terms => string (525) "aaa22384 rabbit no cross reaction with other factors typical testing data st...
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aaa22384 rabbit no cross reaction with other factors typical testing data standard curve for reference only aaa22384_sc elisa kit intercellular adhesion molecule 1 icam icam1 bb2 cd54 p3.58 cell surface glycoprotein major group rhinovirus receptor human 57,825 da cd_antigen icam1_human 167466198 np_000192.2 p05362 nm_000201.2 q5nkv7 q96b50 b2r6m3 gene 611162 samples serum plasma or culture supernatant assay type quantitative sandwich detection range 10 ng ml 0.156 sensitivity up to 0.05 intra precision molecule1 range10
⇄specificity => string (75) "Specifically recognize PRNP, no obvious cross reaction with other analogues"
$value[10]['_source']['specificity']
⇄purity => string (3) "N/A"
$value[10]['_source']['purity']
⇄form => string (3) "N/A"
$value[10]['_source']['form']
⇄concentration => string (3) "N/A"
$value[10]['_source']['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[10]['_source']['storage_stability']
Store entire kit at 2-8C for short-term. For longer-term, please store the microplate & standard at -20C, while the remaining reagents can be stored at 2-8C
Assay Type||Sandwich!!Samples||Serum, plasma, cell culture supernatant and other biological samples!!Detection Range||0.313-20ng/ml!!Sensitivity||0.188ng/ml
⇄⧉etc_term2 => string (270) "Intra-assay Precision||Intra-assay Precision: samples with low, medium and h...
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Intra-assay Precision||Intra-assay Precision: samples with low, medium and high concentration are tested 20 times on same plate.!!Inter-assay Precision||Inter-assay Precision: samples with low, medium and high concentration are tested 20 times on three different plates.
⇄⧉products_description => string (1500) "Background: The prion protein (PRNP) is a glycoprotein that exists in membra...
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Background: The prion protein (PRNP) is a glycoprotein that exists in membrane-bound and non-membrane-bound forms. PRNP binds copper ion with low affinity and may affect copper metabolism, especially in the central nervous system, where this protein is highly expressed. The interaction between copper and PRNP may have a protective effect on neurons. Diseases associated with PRNP include Creutzfeldt-Jakob Disease and Fatal Familial Insomnia. Among its related pathways are Nervous system development and NCAM signaling for neurite out-growth.<br><br>Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti PRNP antibody was pre-coated onto the 96-well plate. The biotin conjugated anti PRNP antibody was used as the detection antibody. The standards and pilot samples were added to the wells subsequently. After incubation, unbound conjugates were removed by wash buffer. Then, biotinylated detection antibody was added to bind with PRNP conjugated on coated antibody. After washing off unbound conjugates, HRP-Streptavidin was added. After a third washing, TMB substrates were added to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that turned yellow after adding a stop solution. Read the O.D. absorbance at 450nm in a microplate reader. The concentration of PRNP in the sample was calculated by drawing a standard curve. The concentration of the target substance is proportional to the OD450 value.
⇄products_references => string (3) "N/A"
$value[10]['_source']['products_references']
⇄⧉products_related_diseases => string (272) "Prion Diseases||1092!!Nervous System Diseases||1072!!Creutzfeldt-Jakob Syndr...
⇄⧉search_terms => string (661) "aaa17478 human this assay has high sensitivity and excellent specificity for...
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aaa17478 human this assay has high sensitivity and excellent specificity for detection of prnp no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17478_sc elisa kit major prion protein prp33 35c ascr prp27 30 cjd gss prp kuru prip prpc cd230 altprp p27 preproprotein alternative 8,691 da cd_antigen prio_human 122056628 np_001073592.1 p04156 f7vjq1 nm_001080123.1 o60489 p78446 q15216 q15221 q27h91 q5qpb4 q8tbg0 q96e70 q9up19 123400 samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 0.313 20ng ml 0.188ng intra precision cv prp2730
⇄⧉specificity => string (169) "This assay has high sensitivity and excellent specificity for detection of P...
$value[11]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PRG2. No significant cross-reactivity or interference between PRG2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[11]['_source']['purity']
⇄form => string (3) "N/A"
$value[11]['_source']['form']
⇄concentration => string (3) "N/A"
$value[11]['_source']['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[11]['_source']['storage_stability']
Store entire kit at 2-8C for short-term. For longer-term, please store the microplate & standard at -20C, while the remaining reagents can be stored at 2-8C
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[11]['_source']['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄products_references => string (3) "N/A"
$value[11]['_source']['products_references']
⇄⧉products_related_diseases => string (192) "Immune System Diseases||5!!Hypertension||3!!Inflammation||3!!Lung Diseases||...
⇄⧉search_terms => string (648) "aaa17367 human this assay has high sensitivity and excellent specificity for...
$value[11]['_source']['search_terms']
aaa17367 human this assay has high sensitivity and excellent specificity for detection of prg2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17367_sc elisa kit bone marrow proteoglycan bmpg 2 isoform 1 preproprotein natural killer cell activator eosinophil granule major basic protein mbp mbp1 23,901 da embp prg2_human 727346123 np_001289856.1 p13727 nm_001302927.1 p81448 q14227 q6ict2 a6xmw0 b2r5i1 605601 samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 0.313 20ng ml 0.188ng intra precision cv bmpg2 isoform1
⇄⧉products_description => string (828) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[12]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Human ICAM-1 monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄⧉search_terms => string (517) "aaa12804 human no cross reaction with other factors typical testing data sta...
$value[12]['_source']['search_terms']
aaa12804 human no cross reaction with other factors typical testing data standard curve for reference only aaa12804_sc elisa kit intercellular adhesion molecule 1 icam icam1 bb2 cd54 p3.58 cell surface glycoprotein major group rhinovirus receptor 57,825 da cd_antigen icam1_human 167466198 np_000192.2 p05362 nm_000201.2 q5nkv7 q96b50 b2r6m3 gene 611162 samples serum plasma or culture supernatant assay type quantitative sandwich detection range 5000 pg ml 78 sensitivity up to 20 intra precision molecule1 ml78 to20
⇄⧉specificity => string (187) "This assay has high sensitivity and excellent specificity for detection of h...
$value[13]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human HLA-DRA. No significant cross-reactivity or interference between human HLA-DRA and analogues was observed.
⇄purity => string (3) "N/A"
$value[13]['_source']['purity']
⇄form => string (3) "N/A"
$value[13]['_source']['form']
⇄concentration => string (3) "N/A"
$value[13]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[13]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[13]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄products_price => string (6) "0.0000"
$value[13]['_source']['products_price']
⇄products_weight => string (4) "5.00"
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⇄products_status => boolean true
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⇄products_tax_class_id => string (1) "1"
$value[13]['_source']['products_tax_class_id']
⇄manufacturers_id => string (3) "700"
$value[13]['_source']['manufacturers_id']
⇄products_ordered => string (1) "0"
$value[13]['_source']['products_ordered']
⇄language_id => string (1) "1"
$value[13]['_source']['language_id']
⇄products_name => string (55) "HLA class II histocompatibility antigen, DR alpha chain"
$value[13]['_source']['products_name']
⇄⧉products_name_oem => string (80) "Human HLA class II histocompatibility antigen, DR alpha chain, HLA-DRA ELISA...
$value[13]['_source']['products_name_oem']
Human HLA class II histocompatibility antigen, DR alpha chain, HLA-DRA ELISA Kit
⇄⧉products_name_syn => string (356) "Human HLA class II histocompatibility antigen; DR alpha chain (HLA-DRA) ELIS...
$value[13]['_source']['products_name_syn']
Human HLA class II histocompatibility antigen; DR alpha chain (HLA-DRA) ELISA kit; DASS-397D15.1; HLA-DRA1; HLA class II histocompatibility antigen; DR alpha chain; MHC cell surface glycoprotein; histocompatibility antigen HLA-DR alpha major histocompatibility complex; class II; DR alpha (HLA-DRA) ; HLA class II histocompatibility antigen; DR alpha chain
⇄products_gene_name => string (7) "HLA-DRA"
$value[13]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (743) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[13]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for HLA-DRA has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any HLA-DRA present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for HLA-DRA is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of HLA-DRA bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
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⇄⧉products_related_diseases => string (219) "Nervous System Diseases||72!!Skin Diseases||47!!Multiple Sclerosis||43!!Necr...
⇄ncbi_full_name => string (55) "HLA class II histocompatibility antigen, DR alpha chain"
$value[13]['_source']['ncbi_full_name']
⇄ncbi_full_name_syn => string (52) "major histocompatibility complex, class II, DR alpha"
$value[13]['_source']['ncbi_full_name_syn']
⇄ncbi_symbol => string (7) "HLA-DRA"
$value[13]['_source']['ncbi_symbol']
⇄ncbi_symbol_syn => string (14) "MLRW; HLA-DRA1"
$value[13]['_source']['ncbi_symbol_syn']
⇄⧉ncbi_protein_info => string (153) "HLA class II histocompatibility antigen, DR alpha chain; MHC class II antige...
$value[13]['_source']['ncbi_protein_info']
HLA class II histocompatibility antigen, DR alpha chain; MHC class II antigen DRA; MHC cell surface glycoprotein; histocompatibility antigen HLA-DR alpha
⇄ncbi_chrom_loc => string (3) "N/A"
$value[13]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (4) "3122"
$value[13]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (9) "28,607 Da"
$value[13]['_source']['ncbi_mol_weight']
⇄⧉ncbi_pathways => string (375) "Adaptive Immune System Pathway||366160!!Allograft Rejection Pathway||920963!...
$value[13]['_source']['ncbi_pathways']
Adaptive Immune System Pathway||366160!!Allograft Rejection Pathway||920963!!Allograft Rejection Pathway||83123!!Allograft Rejection Pathway||535!!Antigen Processing And Presentation Pathway||83074!!Antigen Processing And Presentation Pathway||485!!Asthma Pathway||83120!!Asthma Pathway||532!!Autoimmune Thyroid Disease Pathway||83121!!Autoimmune Thyroid Disease Pathway||533
⇄sp_protein_name => string (55) "HLA class II histocompatibility antigen, DR alpha chain"
$value[13]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (24) "MHC class II antigen DRA"
⇄⧉search_terms => string (565) "aaa15886 human this assay has high sensitivity and excellent specificity for...
$value[13]['_source']['search_terms']
aaa15886 human this assay has high sensitivity and excellent specificity for detection of hla dra no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15886_td elisa kit class ii histocompatibility antigen dr alpha chain dass 397d15.1 dra1 mhc cell surface glycoprotein major complex mlrw 28,607 da dra_human 52426774 np_061984.2 p01903 nm_019111.4 q30160 q6iaz1 q861i2 q9tp70 a2bet4 gene 610424 samples serum plasma tissue homogenates type quantitative sandwich range 18.75 pg ml 1200
⇄⧉specificity => string (171) "This assay has high sensitivity and excellent specificity for detection of I...
$value[14]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of ITIH4. No significant cross-reactivity or interference between ITIH4 and analogues was observed.
⇄purity => string (3) "N/A"
$value[14]['_source']['purity']
⇄form => string (3) "N/A"
$value[14]['_source']['form']
⇄concentration => string (3) "N/A"
$value[14]['_source']['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[14]['_source']['storage_stability']
Store entire kit at 2-8C for short-term. For longer-term, please store the microplate & standard at -20C, while the remaining reagents can be stored at 2-8C
ITIH4/gp120/PK-120/H4P/IHRP/ITI-HC4/ITIHL1/PK120/heavy chain-like; 1/inter-alpha (globulin) inhibitor H4 (plasma Kallikrein-sensitive glycoprotein)/inter-alpha-trypsin inhibitor family heavy chain-related protein/inter-alpha-trypsin inhibitor heavy chain H4/plasma kallikrein-sensitive glycoprotein 120
⇄products_gene_name => string (5) "ITIH4"
$value[14]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[14]['_source']['products_gene_name_syn']
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[14]['_source']['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄⧉search_terms => string (657) "aaa17680 human this assay has high sensitivity and excellent specificity for...
$value[14]['_source']['search_terms']
aaa17680 human this assay has high sensitivity and excellent specificity for detection of itih4 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17680_sc elisa kit inter alpha trypsin inhibitor heavy chain h4 gp120 pk 120 h4p ihrp iti hc4 itihl1 pk120 like 1 globulin plasma kallikrein sensitive glycoprotein family related protein 102,146 da major acute phase map 4 itih4_pig 48374067 np_001001537.1 p79263 nm_001001537.1 samples serum tissue homogenates other biological fluids type quantitative sandwich range 3.125 200ng ml 1.875ng intra precision cv<8 cv<10 like1 map4
⇄⧉products_description => string (833) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[15]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Guinea pig MUC5AC monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
mucin-5AC; mucin 5AC, oligomeric mucus/gel-forming; gastric mucin; tracheobronchial mucin; major airway glycoprotein; lewis B blood group antigen; mucin-5 subtype AC, tracheobronchial; mucin 5AC, oligomeric mucus/gel-forming pseudogene; mucin 5, subtypes A and C, tracheobronchial/gastric
⇄ncbi_chrom_loc => string (3) "N/A"
$value[15]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (4) "4586"
$value[15]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (10) "526,608 Da"
$value[15]['_source']['ncbi_mol_weight']
⇄⧉ncbi_pathways => string (239) "Metabolism Of Proteins Pathway||106230!!O-linked Glycosylation Pathway||9804...
$value[15]['_source']['ncbi_pathways']
Metabolism Of Proteins Pathway||106230!!O-linked Glycosylation Pathway||980459!!O-linked Glycosylation Of Mucins Pathway||530747!!Post-translational Protein Modification Pathway||161012!!Termination Of O-glycan Biosynthesis Pathway||530748
⇄sp_protein_name => string (9) "Mucin-5AC"
$value[15]['_source']['sp_protein_name']
⇄⧉sp_protein_name_syn => string (141) "Gastric mucin; Lewis B blood group antigen; LeB; Major airway glycoprotein; ...
$value[15]['_source']['sp_protein_name_syn']
Gastric mucin; Lewis B blood group antigen; LeB; Major airway glycoprotein; Mucin-5 subtype AC, tracheobronchial; Tracheobronchial mucin; TBM
⇄⧉search_terms => string (572) "aaa12764 guinea pig typical testing data standard curve for reference only a...
$value[15]['_source']['search_terms']
aaa12764 guinea pig typical testing data standard curve for reference only aaa12764_sc elisa kit mucin 5 subtype ac muc5ac 5ac oligomeric mucus gel forming tbm leb muc5 gastric tracheobronchial major airway glycoprotein lewis b blood group antigen pseudogene subtypes a and c 526,608 da muc muc5a_human 160370004 p98088.3 p98088 o60460 o76065 q13792 q14425 q658q1 q7m4s5 q8n4m9 q8wwq3 q8wwq4 q8wwq5 158373 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 10 ng ml 0.156 sensitivity up to 0.05 intra precision mucin5 range10
⇄⧉products_description => string (827) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[16]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Human HLA-E monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄products_references => string (3) "N/A"
$value[16]['_source']['products_references']
⇄⧉products_related_diseases => string (217) "Carcinoma||13!!Nervous System Diseases||8!!Skin Diseases||7!!Cardiovascular ...
⇄⧉ncbi_protein_info => string (156) "HLA class I histocompatibility antigen, alpha chain F; HLA F antigen; leukoc...
$value[16]['_source']['ncbi_protein_info']
HLA class I histocompatibility antigen, alpha chain F; HLA F antigen; leukocyte antigen F; HLA class I molecule; MHC class Ib antigen; MHC class I antigen F
⇄ncbi_chrom_loc => string (3) "N/A"
$value[16]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (4) "3134"
$value[16]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (9) "50,438 Da"
$value[16]['_source']['ncbi_mol_weight']
⇄⧉ncbi_pathways => string (478) "Adaptive Immune System Pathway||366160!!Allograft Rejection Pathway||920963!...
$value[16]['_source']['ncbi_pathways']
Adaptive Immune System Pathway||366160!!Allograft Rejection Pathway||920963!!Allograft Rejection Pathway||83123!!Allograft Rejection Pathway||535!!Antigen Presentation: Folding, Assembly And Peptide Loading Of Class I MHC Pathway||366163!!Antigen Processing And Presentation Pathway||83074!!Antigen Processing And Presentation Pathway||485!!Antigen Processing-Cross Presentation Pathway||477122!!Autoimmune Thyroid Disease Pathway||83121!!Autoimmune Thyroid Disease Pathway||533
⇄sp_protein_name => string (53) "HLA class I histocompatibility antigen, alpha chain F"
$value[16]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (64) "CDA12; HLA F antigen; Leukocyte antigen F; MHC class I antigen F"
⇄⧉search_terms => string (521) "aaa12527 human no cross reaction with other factors typical testing data sta...
$value[16]['_source']['search_terms']
aaa12527 human no cross reaction with other factors typical testing data standard curve for reference only aaa12527_sc elisa kit leukocyte antigen e hla f major histocompatibility complex class i hlaf cda12 5.4 alpha chain molecule mhc ib 50,438 da hlaf_human 312407 caa34947.1 p30511 q5jqi8 q5jqj1 q5spt5 q860r0 q8mgq1 q8wlp5 q95hc0 q9tp68 143110 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 200 u ml 3.12 sensitivity up to 0.6 intra precision cda125.4 range200 to0.6
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value[17]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human AKAP4. No significant cross-reactivity or interference between human AKAP4 and analogues was observed.
⇄purity => string (3) "N/A"
$value[17]['_source']['purity']
⇄form => string (3) "N/A"
$value[17]['_source']['form']
⇄concentration => string (3) "N/A"
$value[17]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[17]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[17]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄products_price => string (6) "0.0000"
$value[17]['_source']['products_price']
⇄products_weight => string (4) "5.00"
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⇄products_status => boolean true
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⇄products_tax_class_id => string (1) "1"
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⇄manufacturers_id => string (3) "700"
$value[17]['_source']['manufacturers_id']
⇄products_ordered => string (1) "0"
$value[17]['_source']['products_ordered']
⇄language_id => string (1) "1"
$value[17]['_source']['language_id']
⇄products_name => string (32) "A kinase (PRKA) anchor protein 4"
Human A-kinase anchor protein 4 (AKAP4) ELISA kit; RP13-377G1__B.1; AKAP82; CT99; FSC1; HI; hAKAP82; p82; A-kinase anchor protein 4; A-kinase anchor protein 82 kDa; cancer/testis antigen 99; protein kinase A anchoring protein 4; testis-specific gene HI; A kinase (PRKA) anchor protein 4
⇄products_gene_name => string (5) "AKAP4"
$value[17]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[17]['_source']['products_gene_name_syn']
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[17]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for AKAP4 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any AKAP4 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for AKAP4 is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of AKAP4 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
$value[17]['_source']['products_references']
⇄⧉products_related_diseases => string (162) "Genital Diseases, Male||19!!Infertility, Male||16!!Immune System Diseases||2...
A-kinase anchor protein 4; testis-specific gene HI; cancer/testis antigen 99; A-kinase anchor protein 82 kDa; major sperm fibrous sheath protein; protein kinase A anchoring protein 4; protein kinase A-anchoring protein 4
⇄ncbi_chrom_loc => string (3) "N/A"
$value[17]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (4) "8852"
$value[17]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (9) "94,477 Da"
$value[17]['_source']['ncbi_mol_weight']
⇄ncbi_pathways => string (36) "G Protein Signaling Pathways||198849"
$value[17]['_source']['ncbi_pathways']
⇄sp_protein_name => string (25) "A-kinase anchor protein 4"
$value[17]['_source']['sp_protein_name']
⇄⧉sp_protein_name_syn => string (133) "A-kinase anchor protein 82 kDa; AKAP 82; hAKAP82; Major sperm fibrous sheath...
$value[17]['_source']['sp_protein_name_syn']
A-kinase anchor protein 82 kDa; AKAP 82; hAKAP82; Major sperm fibrous sheath protein; HI; Protein kinase A-anchoring protein 4; PRKA4
⇄⧉search_terms => string (670) "aaa18226 human this assay has high sensitivity and excellent specificity for...
$value[17]['_source']['search_terms']
aaa18226 human this assay has high sensitivity and excellent specificity for detection of akap4 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18226_td elisa kit a kinase prka anchor protein 4 rp13 377g1__b.1 akap82 ct99 fsc1 hi hakap82 p82 82 kda cancer testis antigen 99 anchoring specific gene isoform 1 prka4 akap major sperm fibrous sheath 94,477 da akap4_human 21493037 np_003877.2 q5jqc9 nm_003886.2 o60904 o95246 q5jqd1 q5jqd2 q5jqd3 a0av85 300185 samples serum plasma tissue homogenates type quantitative sandwich range 25 pg ml 1600 protein4 p8282 antigen99 isoform1 range25
⇄⧉specificity => string (179) "This assay has high sensitivity and excellent specificity for detection of p...
$value[18]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of pig cTn-I. No significant cross-reactivity or interference between pig cTn-I and analogues was observed.
⇄purity => string (3) "N/A"
$value[18]['_source']['purity']
⇄form => string (3) "N/A"
$value[18]['_source']['form']
⇄concentration => string (3) "N/A"
$value[18]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[18]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (326) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[18]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
Rat Cathepsin L1 (CTSL1) ELISA kit; CATL; CTSL; FLJ31037; MEP; cathepsin L; major excreted protein; cathepsin L1
⇄products_gene_name => string (5) "CTSL1"
$value[18]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[18]['_source']['products_gene_name_syn']
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[18]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for cTn-I has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any cTn-I present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for cTn-I is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of cTn-I bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
$value[18]['_source']['products_references']
⇄⧉products_related_diseases => string (224) "Nervous System Diseases||48!!Gastrointestinal Diseases||40!!Brain Diseases||...
⇄⧉search_terms => string (637) "aaa18186 rat this assay has high sensitivity and excellent specificity for d...
$value[18]['_source']['search_terms']
aaa18186 rat this assay has high sensitivity and excellent specificity for detection of pig ctn i no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18186_td elisa kit cathepsin l1 ctsl1 catl ctsl flj31037 mep l major excreted protein preproprotein cathl cp 2 cyclic 37,660 da catl1_rat 6978723 np_037288.1 p07154 nm_013156.2 q9qv07 samples serum plasma tissue homogenates type quantitative sandwich range 15.6 pg ml 1000 3.9 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in cp2
⇄⧉products_description => string (828) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[19]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Human MUC5AC monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
mucin-5AC; mucin 5AC, oligomeric mucus/gel-forming; gastric mucin; tracheobronchial mucin; major airway glycoprotein; lewis B blood group antigen; mucin-5 subtype AC, tracheobronchial; mucin 5AC, oligomeric mucus/gel-forming pseudogene; mucin 5, subtypes A and C, tracheobronchial/gastric
⇄ncbi_chrom_loc => string (3) "N/A"
$value[19]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (4) "4586"
$value[19]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (10) "526,608 Da"
$value[19]['_source']['ncbi_mol_weight']
⇄⧉ncbi_pathways => string (239) "Metabolism Of Proteins Pathway||106230!!O-linked Glycosylation Pathway||9804...
$value[19]['_source']['ncbi_pathways']
Metabolism Of Proteins Pathway||106230!!O-linked Glycosylation Pathway||980459!!O-linked Glycosylation Of Mucins Pathway||530747!!Post-translational Protein Modification Pathway||161012!!Termination Of O-glycan Biosynthesis Pathway||530748
⇄sp_protein_name => string (9) "Mucin-5AC"
$value[19]['_source']['sp_protein_name']
⇄⧉sp_protein_name_syn => string (141) "Gastric mucin; Lewis B blood group antigen; LeB; Major airway glycoprotein; ...
$value[19]['_source']['sp_protein_name_syn']
Gastric mucin; Lewis B blood group antigen; LeB; Major airway glycoprotein; Mucin-5 subtype AC, tracheobronchial; Tracheobronchial mucin; TBM
⇄⧉search_terms => string (606) "aaa12647 human no cross reaction with other factors typical testing data sta...
$value[19]['_source']['search_terms']
aaa12647 human no cross reaction with other factors typical testing data standard curve for reference only aaa12647_td elisa kit mucin 5 subtype ac muc5ac 5ac oligomeric mucus gel forming tbm leb muc5 gastric tracheobronchial major airway glycoprotein lewis b blood group antigen pseudogene subtypes a and c 526,608 da muc muc5a_human 160370004 p98088.3 p98088 o60460 o76065 q13792 q14425 q658q1 q7m4s5 q8n4m9 q8wwq3 q8wwq4 q8wwq5 158373 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 5000 pg ml 78 sensitivity 20 intra precision mucin5 ml78 sensitivity20
