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` = '29163'
AND `pd`.`language_id` = 1
LIMIT 1
Query
Database
1.88 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 = '29163' and pd.language_id = 1
Query
Database
1.65 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` = '29163'
Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
2.84 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` = '29163'
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 = '29163' 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` = '29163'
IHC (Immunohistochemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC7.jpg!!IHC (Immunohistchemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC6.jpg!!Application Data||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_APP5.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC4.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC3.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC2.jpg!!WB (Western Blot)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_WB.jpg
⇄⧉ncbi_pathways => string (394) "Carbohydrate Digestion And Absorption Pathway||170720!!Carbohydrate Digestio...
$value['ncbi_pathways']
Carbohydrate Digestion And Absorption Pathway||170720!!Carbohydrate Digestion And Absorption Pathway||170654!!Digestion Of Dietary Carbohydrate Pathway||106197!!Metabolism Pathway||477135!!Metabolism Of Carbohydrates Pathway||106196!!Salivary Secretion Pathway||153376!!Salivary Secretion Pathway||153352!!Starch And Sucrose Metabolism Pathway||82974!!Starch And Sucrose Metabolism Pathway||344
IHC (Immunohistochemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC7.jpg!!IHC (Immunohistchemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC6.jpg!!Application Data||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_APP5.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC4.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC3.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC2.jpg!!WB (Western Blot)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_WB.jpg
⇄⧉ncbi_pathways => string (394) "Carbohydrate Digestion And Absorption Pathway||170720!!Carbohydrate Digestio...
$value->a['ncbi_pathways']
Carbohydrate Digestion And Absorption Pathway||170720!!Carbohydrate Digestion And Absorption Pathway||170654!!Digestion Of Dietary Carbohydrate Pathway||106197!!Metabolism Pathway||477135!!Metabolism Of Carbohydrates Pathway||106196!!Salivary Secretion Pathway||153376!!Salivary Secretion Pathway||153352!!Starch And Sucrose Metabolism Pathway||82974!!Starch And Sucrose Metabolism Pathway||344
IHC (Immunohistochemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC7.jpg!!IHC (Immunohistchemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC6.jpg!!Application Data||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_APP5.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC4.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC3.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC2.jpg!!WB (Western Blot)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_WB.jpg
⇄⧉ncbi_pathways => string (394) "Carbohydrate Digestion And Absorption Pathway||170720!!Carbohydrate Digestio...
$value->d['ncbi_pathways']
Carbohydrate Digestion And Absorption Pathway||170720!!Carbohydrate Digestion And Absorption Pathway||170654!!Digestion Of Dietary Carbohydrate Pathway||106197!!Metabolism Pathway||477135!!Metabolism Of Carbohydrates Pathway||106196!!Salivary Secretion Pathway||153376!!Salivary Secretion Pathway||153352!!Starch And Sucrose Metabolism Pathway||82974!!Starch And Sucrose Metabolism Pathway||344
IHC (Immunohistochemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC7.jpg!!IHC (Immunohistchemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC6.jpg!!Application Data||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_APP5.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC4.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC3.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_IHC2.jpg!!WB (Western Blot)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29163_WB.jpg
⇄⧉ncbi_pathways => string (394) "Carbohydrate Digestion And Absorption Pathway||170720!!Carbohydrate Digestio...
$value[0]['_source']['ncbi_pathways']
Carbohydrate Digestion And Absorption Pathway||170720!!Carbohydrate Digestion And Absorption Pathway||170654!!Digestion Of Dietary Carbohydrate Pathway||106197!!Metabolism Pathway||477135!!Metabolism Of Carbohydrates Pathway||106196!!Salivary Secretion Pathway||153376!!Salivary Secretion Pathway||153352!!Starch And Sucrose Metabolism Pathway||82974!!Starch And Sucrose Metabolism Pathway||344
⇄⧉products_description => string (674) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
$value[1]['_source']['products_description']
Principle of the Assay: This experiment use double-sandwich elisa technique and the ELISA Kit provided is typical. The pre-coated antibody is human AMY 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.
⇄⧉ncbi_pathways => string (115) "Metabolic Pathways||132021!!Starch And Sucrose Metabolism Pathway||3012!!Sta...
$value[1]['_source']['ncbi_pathways']
Metabolic Pathways||132021!!Starch And Sucrose Metabolism Pathway||3012!!Starch And Sucrose Metabolism Pathway||344
⇄sp_protein_name => string (3) "N/A"
$value[1]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (3) "N/A"
$value[1]['_source']['sp_protein_name_syn']
⇄sp_gene_name => string (3) "N/A"
$value[1]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (3) "N/A"
$value[1]['_source']['sp_gene_name_syn']
⇄sp_entry_name => string (3) "N/A"
$value[1]['_source']['sp_entry_name']
⇄sp_mim => string (3) "N/A"
$value[1]['_source']['sp_mim']
⇄sp_interactions => string (3) "N/A"
$value[1]['_source']['sp_interactions']
⇄products_url => string (3) "N/A"
$value[1]['_source']['products_url']
⇄products_viewed => string (1) "0"
$value[1]['_source']['products_viewed']
⇄⧉search_terms => string (497) "aaa12760 human no cross reaction with other factors typical testing data sta...
$value[1]['_source']['search_terms']
aaa12760 human no cross reaction with other factors typical testing data standard curve for reference only aaa12760_td elisa kit amylase proximal isoform b amy p alpha amy1 amy2 amy4 amy5 amya cg18640 cg18730 dmelcg18730 gene product from transcript rb pa pb a 665401544 np_001286518.1 nm_001299589.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 100 ng ml 1.56ng sensitivity 0.5 intra precision <= 8 inter 12 range100 sensitivity0.5 <=8 inter12
⇄⧉specificity => string (181) "This assay has high sensitivity and excellent specificity for detection of h...
$value[2]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human AMY1. No significant cross-reactivity or interference between human AMY1 and analogues was observed.
⇄purity => string (3) "N/A"
$value[2]['_source']['purity']
⇄form => string (3) "N/A"
$value[2]['_source']['form']
⇄concentration => string (3) "N/A"
$value[2]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[2]['_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[2]['_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_description => string (731) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[2]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for AMY1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any AMY1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for AMY1 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 AMY1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (574) "aaa15378 human this assay has high sensitivity and excellent specificity for...
$value[2]['_source']['search_terms']
aaa15378 human this assay has high sensitivity and excellent specificity for detection of amy1 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15378_td elisa kit alpha amylase 1 4 d glucan glucanohydrolase salivary amy1a amy1b amy1c 1b glycogenase 1,4 57,768 da amy1amy1b amy1amy1c amy1_human 56549662 np_001008219.1 p04745 nm_001008218.1 q13763 q5t083 a6njs5 a8k8h6 gene 104702 samples serum saliva tissue homogenates type quantitative sandwich range 7.8 iu ml 500 amylase1 range7.8 ml500
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||1-300ng/ml!!Sensitivity||0.54ng/ml
⇄⧉etc_term2 => string (403) "Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Thr...
$value[3]['_source']['etc_term2']
Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision. Intra-Assay: CV<8%!!Inter-assay Precision||Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision. CV(%) = SD/mean x 100. Inter-Assay: CV<10%
⇄⧉products_description => string (897) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[3]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Fish AMS;AMY antibody. AMS;AMY present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Fish AMS;AMY Antibody is added and binds to AMS;AMY in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated AMS;AMY antibody. After incubation unbound Streptavidin-HRP is washed away during a washing step. Substrate solution is then added and color develops in proportion to the amount of Fish AMS;AMY. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.<br><br>Intended Uses: This sandwich kit is for the accurate quantitative detection of Fish alpha-amylase (also known as AMS;AMY) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉search_terms => string (496) "aaa18984 fish typical testing data standard curve for reference only aaa1898...
$value[3]['_source']['search_terms']
aaa18984 fish typical testing data standard curve for reference only aaa18984_sc elisa kit alpha amylase amy sco7019 aml 21225304 np_631083.1 nc_003888.3 samples serum plasma cell culture supernates ascites tissue homogenates or other biological fluids assay type quantitative sandwich detection range 1 300ng ml sensitivity 0.54ng intra precision within an three of known concentration were tested on one plate to assess cv<8 inter between assays in separate cv = sd mean x 100 cv<10 range1 x100
⇄⧉products_description => string (673) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
$value[4]['_source']['products_description']
Principle of the Assay: This experiment use double-sandwich elisa technique and the ELISA Kit provided is typical. The pre-coated antibody is Rat PAMY 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.
⇄⧉ncbi_pathways => string (226) "Carbohydrate Digestion And Absorption Pathway||170716!!Carbohydrate Digestio...
$value[4]['_source']['ncbi_pathways']
Carbohydrate Digestion And Absorption Pathway||170716!!Carbohydrate Digestion And Absorption Pathway||170654!!Metabolic Pathways||132933!!Starch And Sucrose Metabolism Pathway||83366!!Starch And Sucrose Metabolism Pathway||344
⇄⧉search_terms => string (456) "aaa13141 rat no cross reaction with other factors typical testing data stand...
$value[4]['_source']['search_terms']
aaa13141 rat no cross reaction with other factors typical testing data standard curve for reference only aaa13141_sc elisa kit pancreatic amylase pamy alpha 2a3 amy2a3 amy2 pa 2 1,4 d glucan glucanohydrolase 57,177 da amyp_rat 13928684 np_113690.1 p00689 nm_031502.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 20 ng ml 0.312 sensitivity up to 0.06 intra precision <= 8 inter 12 pa2 range20 <=8 inter12
⇄⧉products_description => string (826) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[5]['_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-Mouse PAMY 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.
⇄⧉ncbi_pathways => string (226) "Carbohydrate Digestion And Absorption Pathway||170716!!Carbohydrate Digestio...
$value[5]['_source']['ncbi_pathways']
Carbohydrate Digestion And Absorption Pathway||170716!!Carbohydrate Digestion And Absorption Pathway||170654!!Metabolic Pathways||132933!!Starch And Sucrose Metabolism Pathway||83366!!Starch And Sucrose Metabolism Pathway||344
⇄⧉search_terms => string (450) "aaa13019 mouse no cross reaction with other factors typical testing data sta...
$value[5]['_source']['search_terms']
aaa13019 mouse no cross reaction with other factors typical testing data standard curve for reference only aaa13019_sc elisa kit pancreatic amylase pamy alpha 2a3 amy2a3 amy2 pa 2 1,4 d glucan glucanohydrolase 57,177 da amyp_rat 13928684 np_113690.1 p00689 nm_031502.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 u l 15.6 sensitivity up to 5 intra precision <= 8 inter 12 pa2 to5 <=8 inter12
⇄⧉testing_protocols => string (845) "IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded human ...
$value[6]['_source']['testing_protocols']
IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded human liver using MANF antibody at dilution of 1:100 (40x lens).||AAA14841_IHC7.jpg!!IHC (Immunohistchemistry)||Immunohistochemistry of paraffin-embedded human liver using MANF antibody at dilution of 1:100 (40x lens).||AAA14841_IHC6.jpg!!Application Data||AAA14841_APP5.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded human liver using MANF antibody at dilution of 1:100 (40x lens).||AAA14841_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded human liver using MANF antibody at dilution of 1:100 (40x lens).||AAA14841_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemistry of paraffin-embedded human liver using MANF antibody at dilution of 1:100 (40x lens).||AAA14841_IHC2.jpg!!Application Data||AAA14841_APP.jpg
⇄⧉products_description => string (376) "Exoenzyme that releases successive maltose units from the nonreducing end of...
$value[6]['_source']['products_description']
Exoenzyme that releases successive maltose units from the nonreducing end of a polysaccharide chain by hydrolysis of a 1,4-glucan linkages. The shortest normal saccharide attacked is maltotetraose. Since it is unable to bypass branch linkages in branched polysaccharides such as glycogen or amylopectin, the hydrolysis is incomplete and a macromolecular limit dextrin remains.
⇄⧉etc_term1 => string (174) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
$value[7]['_source']['etc_term1']
Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Competitive or Sandwich!!Detection Range||5.0-100ng/mL!!Sensitivity||1.0ng/mL
⇄⧉products_description => string (1495) "Intended Uses: This SAalpha1 ELISA kit is a 1.5 hour solid-phase ELISA desig...
$value[7]['_source']['products_description']
Intended Uses: This SAalpha1 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human SAalpha1. This ELISA kit for research use only!<br><br>Principle of the Assay: SAalpha1 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for SAalpha1. Standards or samples are then added to the microtiter plate wells and SAalpha1 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of SAalpha1 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for SAalpha1 are added to each well to "sandwich" the SAalpha1 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 SAalpha1 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 SAalpha1 concentration in each sample is interpolated from this standard curve.
⇄products_references => string (3) "N/A"
$value[7]['_source']['products_references']
⇄products_related_diseases => string (3) "N/A"
$value[7]['_source']['products_related_diseases']
⇄products_categories => string (3) "N/A"
$value[7]['_source']['products_categories']
⇄ncbi_full_name => string (13) "AMY1, partial"
$value[7]['_source']['ncbi_full_name']
⇄ncbi_full_name_syn => string (3) "N/A"
$value[7]['_source']['ncbi_full_name_syn']
⇄ncbi_symbol => string (3) "N/A"
$value[7]['_source']['ncbi_symbol']
⇄ncbi_symbol_syn => string (3) "N/A"
$value[7]['_source']['ncbi_symbol_syn']
⇄ncbi_protein_info => string (3) "N/A"
$value[7]['_source']['ncbi_protein_info']
⇄ncbi_chrom_loc => string (3) "N/A"
$value[7]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (3) "N/A"
$value[7]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (9) "15,337 Da"
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aaa16245 human typical testing data standard curve for reference only aaa16245_sc elisa kit amylase alpha 1 salivary amy1 partial 15,337 da c1krz2_bradi 226407125 aco52697.1 samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type competitive or sandwich detection range 5.0 100ng ml sensitivity 1.0ng alpha1 range5.0
IHC (Immunohistchemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29150_IHC6.jpg!!IHC (Immunohistochemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29150_IHC5.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29150_IHC4.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29150_IHC3.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29150_IHC2.jpg!!WB (Western Blot)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29150_WB.jpg
⇄⧉products_description => string (337) "Calcium-dependent lectin that mediates cell adhesion by binding to glycoprot...
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Calcium-dependent lectin that mediates cell adhesion by binding to glycoproteins on neighboring cells (PubMed:28489325, PubMed:28011641). Mediates the adherence of lymphocytes to endothelial cells of high endothelial venules in peripheral lymph nodes. Promotes initial tethering and rolling of leukocytes in endothelia (PubMed:28011641).
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⇄⧉products_related_diseases => string (190) "Nervous System Diseases||202!!Liver Diseases||116!!Inflammation||68!!Pain||6...
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Nervous System Diseases||202!!Liver Diseases||116!!Inflammation||68!!Pain||64!!Heart Diseases||64!!Gastrointestinal Diseases||59!!Necrosis||44!!Kidney Diseases||35!!Fever||27!!Hemorrhage||24
Adaptive Immune System Pathway||366160!!Cell Adhesion Molecules (CAMs) Pathway||83069!!Cell Adhesion Molecules (CAMs) Pathway||480!!Cell Surface Interactions At The Vascular Wall Pathway||106062!!Hemostasis Pathway||106028!!Immune System Pathway||106386!!Immunoregulatory Interactions Between A Lymphoid And A Non-Lymphoid Cell Pathway||106413
⇄sp_protein_name => string (10) "L-selectin"
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⇄⧉sp_protein_name_syn => string (203) "CD62 antigen-like family member L; Leukocyte adhesion molecule 1; LAM-1; Leu...
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||10-3000ng/L!!Sensitivity||5.12ng/L
⇄⧉etc_term2 => string (403) "Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Thr...
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Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision. Intra-Assay: CV<8%!!Inter-assay Precision||Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision. CV(%) = SD/mean x 100. Inter-Assay: CV<10%
⇄⧉products_description => string (904) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
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Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Human L-DOPA antibody. L-DOPA present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Human L-DOPA Antibody is added and binds to L-DOPA in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated L-DOPA antibody. After incubation unbound Streptavidin-HRP is washed away during a washing step. Substrate solution is then added and color develops in proportion to the amount of Human L-DOPA. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.<br><br>Intended Uses: This sandwich kit is for the accurate quantitative detection of Human L-Dihydroxyphenyalanine (also known as L-DOPA) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
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⇄⧉search_terms => string (463) "aaa11181 human typical testing data standard curve for reference only aaa111...
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aaa11181 human typical testing data standard curve for reference only aaa11181_sc elisa kit l dihydroxyphenyalanine dopa samples serum plasma cell culture supernates ascites tissue homogenates or other biological fluids assay type quantitative sandwich detection range 10 3000ng sensitivity 5.12ng intra precision within an three of known concentration were tested on one plate to assess cv<8 inter between assays in separate cv = sd mean x 100 cv<10 range10 x100
⇄⧉products_description => string (676) "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 Mouse L-Arg 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 (335) "aaa22389 mouse no cross reaction with other factors typical testing data sta...
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aaa22389 mouse no cross reaction with other factors typical testing data standard curve for reference only aaa22389_sc elisa kit l arginine arg samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 100 ug ml 1.56 sensitivity up to 0.5 intra precision <= 8 inter 12 range100 to0.5 <=8 inter12
⇄⧉products_description => string (827) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Bovine L-FT 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"
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⇄⧉products_related_diseases => string (297) "Iron Metabolism Disorders||52!!Nervous System Diseases||45!!Brain Diseases||...
⇄⧉ncbi_pathways => string (446) "Binding And Uptake Of Ligands By Scavenger Receptors Pathway||1269897!!Clath...
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Binding And Uptake Of Ligands By Scavenger Receptors Pathway||1269897!!Clathrin Derived Vesicle Budding Pathway||1269881!!Golgi Associated Vesicle Biogenesis Pathway||1269882!!Immune System Pathway||1269170!!Innate Immune System Pathway||1269203!!Integrated Pancreatic Cancer Pathway||711360!!Iron Uptake And Transport Pathway||1269948!!Membrane Trafficking Pathway||1269877!!Mineral Absorption Pathway||212237!!Mineral Absorption Pathway||212220
⇄⧉search_terms => string (415) "aaa22748 bovine typical testing data standard curve for reference only aaa22...
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aaa22748 bovine typical testing data standard curve for reference only aaa22748_sc elisa kit l ferritin ft partial light chain ftl lftd nbia3 20,020 da subunit fril_human 449331665 p02792 q6ibt7 q7z2w1 q86wi9 q8wu07 q96au9 q96cu0 q9btz8 b2r4b9 m11147 mrna samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 20 ng ml 0.312 sensitivity up to 0.06 intra precision range20
⇄⧉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 L-FABP 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 (417) "aaa22370 human no cross reaction with other factors typical testing data sta...
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aaa22370 human no cross reaction with other factors typical testing data standard curve for reference only aaa22370_sc elisa kit liver fatty acid binding protein l fabp 1 fabp1 lfabp 14,192 da q90wa9_chick 14269537 aak58095.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 100 ng ml 1.56 sensitivity up to 0.5 intra precision <= 8 inter 12 range100 to0.5 <=8 inter12
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of S...
$value[13]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of SELP. No significant cross-reactivity or interference between SELP and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between SELP and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
Assay Type||Quantitative Competitive!!Samples||Serum, plasma, cell culture supernatants, body fluid and tissue homogenate!!Sensitivity||1.0 ng/mL
⇄etc_term2 => string (3) "N/A"
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⇄products_price => string (6) "0.0000"
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⇄products_weight => string (4) "5.00"
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⇄products_name => string (10) "P selectin"
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⇄products_name_oem => string (27) "Canine P selectin ELISA Kit"
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⇄products_name_syn => string (3) "N/A"
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⇄products_gene_name => string (2) "PS"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (1391) "Principle of the Assay: SELP ELISA kit applies the competitive enzyme immuno...
$value[13]['_source']['products_description']
Principle of the Assay: SELP ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-SELP antibody and an SELP-HRP conjugate. The assay sample and buffer are incubated together with SELP-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the SELP concentration since SELP from samples and SELP-HRP conjugate compete for the anti-SELP antibody binding site. Since the number of sites is limited, as more sites are occupied by SELP from the sample, fewer sites are left to bind SELP-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The SELP concentration in each sample is interpolated from this standard curve. <br><br>Intended Uses: This SELP ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Canine SELP. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (856) "aaa16965 canine this assay has high sensitivity and excellent specificity fo...
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aaa16965 canine this assay has high sensitivity and excellent specificity for detection of selp no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa16965_sc elisa kit p selectin ps granule membrane protein 140kda antigen cd62 grmp psel cd62p gmp140 lecam3 padgem gmp 140 granulocyte like family member platelet alpha leukocyte endothelial cell adhesion molecule 3 activation dependent external 90,834 da cd_antigen gmrp lyam3_human 157419154 np_002996.2 p16109 nm_003005.3 q5r344 q8ivd1 gene+601367 immunology samples serum plasma culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 ng ml molecule3 competitive1.0
IHC (Immunohistochemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.||AAA29306_IHC7.jpg!!WB (Western Blot)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.||AAA29306_WB6.jpg!!Application Data||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.||AAA29306_APP5.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.||AAA29306_IHC4.jpg!!IHC (Immunohistochemistry-Paraffin)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.||AAA29306_IHC3.jpg!!WB (Western Blot)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.||AAA29306_WB2.jpg!!WB (Western Blot)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-1:300. ELISA: 1/10000. Not yet tested in other applications.||AAA29306_WB.jpg
⇄⧉products_name_syn => string (238) "SELP; GMRP; GRMP; P-selectin; CD62 antigen-like family member P; Granule mem...
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SELP; GMRP; GRMP; P-selectin; CD62 antigen-like family member P; Granule membrane protein 140; GMP-140; Leukocyte-endothelial cell adhesion molecule 3; LECAM3; Platelet activation dependent granule-external membrane protein; PADGEM; CD62P
⇄products_gene_name => string (4) "SELP"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (370) "Ca (2+)-dependent receptor for myeloid cells that binds to carbohydrates on ...
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Ca (2+)-dependent receptor for myeloid cells that binds to carbohydrates on neutrophils and monocytes. Mediates the interaction of activated endothelial cells or platelets with leukocytes. The ligand recognized is sialyl-Lewis X. Mediates rapid rolling of leukocyte rolling over vascular surfaces during the initial steps in inflammation through interaction with SELPLG.
⇄⧉specificity => string (191) "This assay has high sensitivity and excellent specificity for detection of p...
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This assay has high sensitivity and excellent specificity for detection of pig sP-Selectin. No significant cross-reactivity or interference between pig sP-Selectin and analogues was observed.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => 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 (327) "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%<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_description => string (759) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
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Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for sP-Selectin has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any sP-Selectin present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for sP-Selectin 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 sP-Selectin bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (511) "aaa15283 pig this assay has high sensitivity and excellent specificity for d...
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aaa15283 pig this assay has high sensitivity and excellent specificity for detection of sp selectin no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15283_td elisa kit soluble p samples serum plasma cell culture supernates tissue homogenates type quantitative sandwich range 12.5 ng ml 800 <3.12 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in ml800
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of S...
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This assay has high sensitivity and excellent specificity for detection of SELP. No significant cross-reactivity or interference between SELP and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between SELP and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
Assay Type||Quantitative Competitive!!Samples||Serum, plasma, cell culture supernatants, body fluid and tissue homogenate!!Sensitivity||1.0 ng/mL
⇄etc_term2 => string (3) "N/A"
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⇄products_weight => string (4) "5.00"
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⇄products_status => boolean true
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⇄products_name_oem => string (28) "Porcine P selectin ELISA Kit"
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⇄products_gene_name => string (2) "PS"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (1391) "Principle of the Assay: SELP ELISA kit applies the competitive enzyme immuno...
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Principle of the Assay: SELP ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-SELP antibody and an SELP-HRP conjugate. The assay sample and buffer are incubated together with SELP-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the SELP concentration since SELP from samples and SELP-HRP conjugate compete for the anti-SELP antibody binding site. Since the number of sites is limited, as more sites are occupied by SELP from the sample, fewer sites are left to bind SELP-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The SELP concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This SELP ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Porcine SELP. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (857) "aaa16718 porcine this assay has high sensitivity and excellent specificity f...
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aaa16718 porcine this assay has high sensitivity and excellent specificity for detection of selp no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa16718_sc elisa kit p selectin ps granule membrane protein 140kda antigen cd62 grmp psel cd62p gmp140 lecam3 padgem gmp 140 granulocyte like family member platelet alpha leukocyte endothelial cell adhesion molecule 3 activation dependent external 90,834 da cd_antigen gmrp lyam3_human 157419154 np_002996.2 p16109 nm_003005.3 q5r344 q8ivd1 gene+601367 immunology samples serum plasma culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 ng ml molecule3 competitive1.0
⇄⧉products_description => string (1534) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[17]['_source']['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti- E-Selectin polyclonal antibody was pre-coated onto 96-well plates. And the biotin conjugated anti- E-Selectin polyclonal antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and wash with wash buffer. Avidin-Biotin-Peroxidase Complex 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 E-Selectin amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of E-Selectin can be calculated.<br><br>Background/Introduction: E-selectin, also known as CD62 antigen-like family member E (CD62E), endothelial-leukocyte adhesion molecule 1 (ELAM-1), or leukocyte-endothelial cell adhesion molecule 2 (LECAM2), is a cell adhesion molecule expressed only on endothelial cells activated by cytokines. The ELAM gene is present in single copy in the human genome and contains 14 exons spanning about 13 kb of DNA. E-selectin mediates the adhesion of tumor cells to endothelial cells, by binding to E-selectin ligands expressed by neutrophils, monocytes, eosinophils, memory-effector T-like lymphocytes, natural killer cells or cancer cells.
⇄⧉search_terms => string (491) "aaa13507 human quantitative selisa eia for detection of e selectin in serum ...
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aaa13507 human quantitative selisa eia for detection of e selectin in serum plasma body fluids tissue lysates or cell culture supernates typical testing data standard curve reference only aaa13507_sc elisa kit sele elam esel cd62e elam1 lecam2 1 endothelial adhesion molecule cd62 antigen like family member leukocyte 2 66,655 da lyam2_human 187960042 np_000441.2 p16581 nm_000450.2 p16111 a2rrd6 131210 samples assay type sandwich range 62.5 pg ml 4000 sensitivity < 4 lecam21 leukocyte2 <4
⇄⧉specificity => string (197) "This assay has high sensitivity and excellent specificity for detection of r...
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This assay has high sensitivity and excellent specificity for detection of rabbit sP-selectin. No significant cross-reactivity or interference between rabbit sP-selectin and analogues was observed.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄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 ...
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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 (328) "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%<12%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<15%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (656) "Principle of the Assay: This assay employs the competitive inhibition enzyme...
$value[18]['_source']['products_description']
Principle of the Assay: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with sP-selectin. Standards or samples are added to the appropriate microtiter plate wells with Horseradish Peroxidase (HRP) conjugated antibody preparation specific for sP-selectin. The competitive inhibition reaction is launched between with pre-coated sP-selectin and sP-selectin in samples. A substrate solution is added to the wells and the color develops in opposite to the amount of sP-selectin in the samples. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (532) "aaa15452 rabbit this assay has high sensitivity and excellent specificity fo...
$value[18]['_source']['search_terms']
aaa15452 rabbit this assay has high sensitivity and excellent specificity for detection of sp selectin no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15452_td elisa kit soluble p samples serum plasma cell culture supernates urine saliva tissue homogenates type quantitative competitive range 31.25 pg ml 2000 < 7.8 intra precision within an cv <12 three known concentration were tested twenty times on one plate to assess inter assays <15 in <7.8
⇄⧉specificity => string (373) "This assay has high sensitivity and excellent specificity for detection of L...
$value[19]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of LAG. No significant cross-reactivity or interference between LAG and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between LAG and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
$value[19]['_source']['form']
⇄concentration => string (3) "N/A"
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
Assay Type||Quantitative Competitive!!Samples||Serum, plasma, cell culture supernatants, body fluid and tissue homogenate!!Sensitivity||0.1 ug/mL
⇄etc_term2 => string (3) "N/A"
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⇄products_price => string (6) "0.0000"
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⇄products_weight => string (4) "5.00"
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⇄products_tax_class_id => string (1) "1"
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⇄manufacturers_id => string (3) "720"
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⇄language_id => string (1) "1"
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⇄products_name => string (10) "L Arginine"
$value[19]['_source']['products_name']
⇄products_name_oem => string (26) "Human L Arginine ELISA Kit"
$value[19]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[19]['_source']['products_name_syn']
⇄products_gene_name => string (2) "LA"
$value[19]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[19]['_source']['products_gene_name_syn']
⇄⧉products_description => string (1376) "Principle of the Assay: LAG ELISA kit applies the competitive enzyme immunoa...
$value[19]['_source']['products_description']
Principle of the Assay: LAG ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-LAG antibody and an LAG-HRP conjugate. The assay sample and buffer are incubated together with LAG-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the LAG concentration since LAG from samples and LAG-HRP conjugate compete for the anti-LAG antibody binding site. Since the number of sites is limited, as more sites are occupied by LAG from the sample, fewer sites are left to bind LAG-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The LAG concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This LAG ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human LAG. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (505) "aaa16439 human this assay has high sensitivity and excellent specificity for...
$value[19]['_source']['search_terms']
aaa16439 human this assay has high sensitivity and excellent specificity for detection of larg no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa16439_sc elisa kit l arginine la samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1ug ml
