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` = '29198'
AND `pd`.`language_id` = 1
LIMIT 1
Query
Database
10.81 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 = '29198' and pd.language_id = 1
Query
Database
4.74 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` = '29198'
Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
5.29 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` = '29198'
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 = '29198' 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` = '29198'
IHC (Immunohistchemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29198_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.||AAA29198_IHC5.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.||AAA29198_WB4.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.||AAA29198_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.||AAA29198_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.||AAA29198_WB.jpg
⇄⧉products_name_syn => string (164) "CD84; SLAMF5; SLAM family member 5; Cell surface antigen MAX.3; Hly9-beta; L...
$value['products_name_syn']
CD84; SLAMF5; SLAM family member 5; Cell surface antigen MAX.3; Hly9-beta; Leukocyte differentiation antigen CD84; Signaling lymphocytic activation molecule 5; CD84
⇄products_gene_name => string (4) "CD84"
$value['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value['products_gene_name_syn']
⇄⧉products_description => string (1684) "Self-ligand receptor of the signaling lymphocytic activation molecule (SLAM)...
$value['products_description']
Self-ligand receptor of the signaling lymphocytic activation molecule (SLAM) family. SLAM receptors triggered by homo- or heterotypic cell-cell interactions are modulating the activation and differentiation of a wide variety of immune cells and thus are involved in the regulation and interconnection of both innate and adaptive immune response. Activities are controlled by presence or absence of small cytoplasmic adapter proteins, SH2D1A/SAP and/or SH2D1B/EAT-2. Can mediate natural killer (NK) cell cytotoxicity dependent on SH2D1A and SH2D1B (By similarity). Increases proliferative responses of activated T- cells and SH2D1A/SAP does not seem be required for this process. Homophilic interactions enhance interferon gamma/IFNG secretion in lymphocytes and induce platelet stimulation via a SH2D1A-dependent pathway. May serve as a marker for hematopoietic progenitor cells (PubMed:12115647. PubMed:12928397, PubMed:12962726, PubMed:16037392) Required for a prolonged T- cell: B-cell contact, optimal T follicular helper function, and germinal center formation. In germinal centers involved in maintaining B-cell tolerance and in preventing autoimmunity (By similarity). In mast cells negatively regulates high affinity immunoglobulin epsilon receptor signaling; independent of SH2D1A and SH2D1B but implicating FES and PTPN6/SHP-1 (PubMed:22068234). In macrophages enhances LPS-induced MAPK phosphorylation and NF- kappaB activation and modulates LPS-induced cytokine secretion; involving ITSM 2 (By similarity). Positively regulates macroautophagy in primary dendritic cells via stabilization of IRF8; inhibits TRIM21-mediated proteasomal degradation of IRF8 (PubMed:29434592).
IHC (Immunohistchemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29198_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.||AAA29198_IHC5.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.||AAA29198_WB4.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.||AAA29198_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.||AAA29198_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.||AAA29198_WB.jpg
⇄⧉products_name_syn => string (164) "CD84; SLAMF5; SLAM family member 5; Cell surface antigen MAX.3; Hly9-beta; L...
$value->a['products_name_syn']
CD84; SLAMF5; SLAM family member 5; Cell surface antigen MAX.3; Hly9-beta; Leukocyte differentiation antigen CD84; Signaling lymphocytic activation molecule 5; CD84
⇄products_gene_name => string (4) "CD84"
$value->a['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value->a['products_gene_name_syn']
⇄⧉products_description => string (1684) "Self-ligand receptor of the signaling lymphocytic activation molecule (SLAM)...
$value->a['products_description']
Self-ligand receptor of the signaling lymphocytic activation molecule (SLAM) family. SLAM receptors triggered by homo- or heterotypic cell-cell interactions are modulating the activation and differentiation of a wide variety of immune cells and thus are involved in the regulation and interconnection of both innate and adaptive immune response. Activities are controlled by presence or absence of small cytoplasmic adapter proteins, SH2D1A/SAP and/or SH2D1B/EAT-2. Can mediate natural killer (NK) cell cytotoxicity dependent on SH2D1A and SH2D1B (By similarity). Increases proliferative responses of activated T- cells and SH2D1A/SAP does not seem be required for this process. Homophilic interactions enhance interferon gamma/IFNG secretion in lymphocytes and induce platelet stimulation via a SH2D1A-dependent pathway. May serve as a marker for hematopoietic progenitor cells (PubMed:12115647. PubMed:12928397, PubMed:12962726, PubMed:16037392) Required for a prolonged T- cell: B-cell contact, optimal T follicular helper function, and germinal center formation. In germinal centers involved in maintaining B-cell tolerance and in preventing autoimmunity (By similarity). In mast cells negatively regulates high affinity immunoglobulin epsilon receptor signaling; independent of SH2D1A and SH2D1B but implicating FES and PTPN6/SHP-1 (PubMed:22068234). In macrophages enhances LPS-induced MAPK phosphorylation and NF- kappaB activation and modulates LPS-induced cytokine secretion; involving ITSM 2 (By similarity). Positively regulates macroautophagy in primary dendritic cells via stabilization of IRF8; inhibits TRIM21-mediated proteasomal degradation of IRF8 (PubMed:29434592).
IHC (Immunohistchemistry)||Dilution: Western Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.||AAA29198_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.||AAA29198_IHC5.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.||AAA29198_WB4.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.||AAA29198_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.||AAA29198_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.||AAA29198_WB.jpg
⇄⧉products_name_syn => string (164) "CD84; SLAMF5; SLAM family member 5; Cell surface antigen MAX.3; Hly9-beta; L...
$value->d['products_name_syn']
CD84; SLAMF5; SLAM family member 5; Cell surface antigen MAX.3; Hly9-beta; Leukocyte differentiation antigen CD84; Signaling lymphocytic activation molecule 5; CD84
⇄products_gene_name => string (4) "CD84"
$value->d['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value->d['products_gene_name_syn']
⇄⧉products_description => string (1684) "Self-ligand receptor of the signaling lymphocytic activation molecule (SLAM)...
$value->d['products_description']
Self-ligand receptor of the signaling lymphocytic activation molecule (SLAM) family. SLAM receptors triggered by homo- or heterotypic cell-cell interactions are modulating the activation and differentiation of a wide variety of immune cells and thus are involved in the regulation and interconnection of both innate and adaptive immune response. Activities are controlled by presence or absence of small cytoplasmic adapter proteins, SH2D1A/SAP and/or SH2D1B/EAT-2. Can mediate natural killer (NK) cell cytotoxicity dependent on SH2D1A and SH2D1B (By similarity). Increases proliferative responses of activated T- cells and SH2D1A/SAP does not seem be required for this process. Homophilic interactions enhance interferon gamma/IFNG secretion in lymphocytes and induce platelet stimulation via a SH2D1A-dependent pathway. May serve as a marker for hematopoietic progenitor cells (PubMed:12115647. PubMed:12928397, PubMed:12962726, PubMed:16037392) Required for a prolonged T- cell: B-cell contact, optimal T follicular helper function, and germinal center formation. In germinal centers involved in maintaining B-cell tolerance and in preventing autoimmunity (By similarity). In mast cells negatively regulates high affinity immunoglobulin epsilon receptor signaling; independent of SH2D1A and SH2D1B but implicating FES and PTPN6/SHP-1 (PubMed:22068234). In macrophages enhances LPS-induced MAPK phosphorylation and NF- kappaB activation and modulates LPS-induced cytokine secretion; involving ITSM 2 (By similarity). Positively regulates macroautophagy in primary dendritic cells via stabilization of IRF8; inhibits TRIM21-mediated proteasomal degradation of IRF8 (PubMed:29434592).
⇄⧉products_description => string (840) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[0]['_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-Porcine ADAMTS-13/vWF-cp 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_protein_info => string (224) "A disintegrin and metalloproteinase with thrombospondin motifs 13; vWF-cleav...
$value[0]['_source']['ncbi_protein_info']
A disintegrin and metalloproteinase with thrombospondin motifs 13; vWF-cleaving protease; von Willebrand factor-cleaving protease; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 13
⇄ncbi_chrom_loc => string (3) "N/A"
$value[0]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (5) "11093"
$value[0]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (9) "39,864 Da"
$value[0]['_source']['ncbi_mol_weight']
⇄⧉ncbi_pathways => string (202) "Metabolism Of Proteins Pathway||106230!!O-glycosylation Of TSR Domain-contai...
$value[0]['_source']['ncbi_pathways']
Metabolism Of Proteins Pathway||106230!!O-glycosylation Of TSR Domain-containing Proteins Pathway||980460!!O-linked Glycosylation Pathway||980459!!Post-translational Protein Modification Pathway||161012
⇄sp_protein_name => string (65) "A disintegrin and metalloproteinase with thrombospondin motifs 13"
⇄⧉search_terms => string (586) "aaa22451 porcine typical testing data standard curve for reference only aaa2...
$value[0]['_source']['search_terms']
aaa22451 porcine typical testing data standard curve for reference only aaa22451_sc elisa kit von willebrand factor cleaving protease adamts 13 vwf cp adam metallopeptidase with thrombospondin type 1 motif adamts13 vwfcp c9orf8 ts13 a disintegrin and metalloproteinase motifs like metalloprotease reprolysin 39,864 da unq6102 pro20085 ts ats13_human 16306598 aal17652.1 q76lx8 q6uy16 q710f6 q711t8 q96l37 q9h0g3 q9ugq1 604134 samples serum plasma or cell culture supernatant assay quantitative sandwich detection range 20 ng ml 0.312 sensitivity up to 0.06 intra precision type1 range20
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of v...
$value[1]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of vWFCP. No significant cross-reactivity or interference between vWFCP and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between vWFCP and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[1]['_source']['purity']
⇄form => string (3) "N/A"
$value[1]['_source']['form']
⇄concentration => string (3) "N/A"
$value[1]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1402) "Principle of the Assay: vWFCP ELISA kit applies the competitive enzyme immun...
$value[1]['_source']['products_description']
Principle of the Assay: vWFCP ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-vWFCP antibody and an vWFCP-HRP conjugate. The assay sample and buffer are incubated together with vWFCP-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 vWFCP concentration since vWFCP from samples and vWFCP-HRP conjugate compete for the anti-vWFCP antibody binding site. Since the number of sites is limited, as more sites are occupied by vWFCP from the sample, fewer sites are left to bind vWFCP-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The vWFCP concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This vWFCP ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Sheep vWFCP. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉ncbi_protein_info => string (224) "A disintegrin and metalloproteinase with thrombospondin motifs 13; vWF-cleav...
$value[1]['_source']['ncbi_protein_info']
A disintegrin and metalloproteinase with thrombospondin motifs 13; vWF-cleaving protease; von Willebrand factor-cleaving protease; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 13
⇄ncbi_chrom_loc => string (3) "N/A"
$value[1]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (5) "11093"
$value[1]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (9) "39,864 Da"
$value[1]['_source']['ncbi_mol_weight']
⇄⧉ncbi_pathways => string (202) "Metabolism Of Proteins Pathway||106230!!O-glycosylation Of TSR Domain-contai...
$value[1]['_source']['ncbi_pathways']
Metabolism Of Proteins Pathway||106230!!O-glycosylation Of TSR Domain-containing Proteins Pathway||980460!!O-linked Glycosylation Pathway||980459!!Post-translational Protein Modification Pathway||161012
⇄sp_protein_name => string (65) "A disintegrin and metalloproteinase with thrombospondin motifs 13"
⇄⧉search_terms => string (901) "aaa16797 sheep this assay has high sensitivity and excellent specificity for...
$value[1]['_source']['search_terms']
aaa16797 sheep this assay has high sensitivity and excellent specificity for detection of vwf cp 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 aaa16797_sc elisa kit von willebrand factor cleaving protease a disintegrin metalloproteinase with thrombospondin motifs 13 isoform 2 preproprotein adam metallopeptidase type 1 motif adamts13 vwfcp c9orf8 ts13 adamts like metalloprotease reprolysin 39,864 da unq6102 pro20085 ts ats13_human 73695936 np_620596.2 q76lx8 nm_139027.4 q6uy16 q710f6 q711t8 q96l37 q9h0g3 q9ugq1 604134 cardiovascular samples serum plasma cell culture supernatants body fluid tissue homogenate quantitative competitive 0.1 ng ml motifs13 isoform2 type1 competitive0.1
⇄⧉products_description => string (826) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[2]['_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-Canine vWF 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 (451) "aaa22651 canine no cross reaction with other factors typical testing data st...
$value[2]['_source']['search_terms']
aaa22651 canine no cross reaction with other factors typical testing data standard curve for reference only aaa22651_sc elisa kit von willebrand factor vwf preproprotein vwd f8vwf 38,745 da antigen 2alternative name s ii vwf_human 89191868 np_000543.2 p04275 nm_000552.3 q8tce8 q99806 193400 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
⇄⧉specificity => string (179) "This assay has high sensitivity and excellent specificity for detection of h...
$value[3]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human vWF. No significant cross-reactivity or interference between human vWF and analogues was observed.
⇄purity => string (3) "N/A"
$value[3]['_source']['purity']
⇄form => string (3) "N/A"
$value[3]['_source']['form']
⇄concentration => string (3) "N/A"
$value[3]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[3]['_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[3]['_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.
Human von Willebrand Factor; vWF ELISA Kit; F8VWF; VWD; coagulation factor VIII VWF; von Willebrand factor
⇄products_gene_name => string (3) "VWF"
$value[3]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[3]['_source']['products_gene_name_syn']
⇄⧉products_description => string (727) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[3]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for vWF has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any vWF present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for vWF 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 vWF bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (529) "aaa15574 human this assay has high sensitivity and excellent specificity for...
$value[3]['_source']['search_terms']
aaa15574 human this assay has high sensitivity and excellent specificity for detection of vwf no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15574_td elisa kit von willebrand factor f8vwf vwd coagulation viii preproprotein 309,265 da antigen ii vwf_human 89191868 np_000543.2 p04275 nm_000552.3 q99806 gene 613554 samples serum plasma tissue homogenates type quantitative sandwich range 6.25 ng ml 400 < 1.56 intra precision within an cv ml400
⇄⧉specificity => string (181) "This assay has high sensitivity and excellent specificity for detection of C...
$value[4]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of Canine VWF. No significant cross-reactivity or interference between Canine VWF and analogues was observed.
⇄purity => string (3) "N/A"
$value[4]['_source']['purity']
⇄form => string (3) "N/A"
$value[4]['_source']['form']
⇄concentration => string (3) "N/A"
$value[4]['_source']['concentration']
⇄storage_stability => string (22) "Store at 2-8 degree C."
$value[4]['_source']['storage_stability']
⇄app_tested => string (3) "N/A"
$value[4]['_source']['app_tested']
⇄app_notes => string (3) "N/A"
$value[4]['_source']['app_notes']
⇄testing_protocols => string (3) "N/A"
$value[4]['_source']['testing_protocols']
⇄⧉etc_term1 => string (179) "Assay Type||Quantitative Sandwich!!Samples||Serum, plasma and other biologic...
$value[4]['_source']['etc_term1']
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma and other biological fluids!!Detection Range||6.25 ng/mL - 400 ng/mL!!Sensitivity||2 ng/mL (mean of 6 independent assays)
⇄⧉etc_term2 => string (420) "Intra-assay Precision||Intra-assay Precision (Precision within an assay) Thr...
$value[4]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty times 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 forty separate assays to assess inter-assay precision. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄products_name_syn => string (39) "F8VWF; VWD; coagulation factor VIII VWF"
$value[4]['_source']['products_name_syn']
⇄products_gene_name => string (3) "VWF"
$value[4]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[4]['_source']['products_gene_name_syn']
⇄⧉products_description => string (900) "Principle of the Assay: This assay employs a two-site sandwich ELISA to quan...
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Principle of the Assay: This assay employs a two-site sandwich ELISA to quantitate VWF in Canine serum, plasma. An antibody specific for VWF has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any VWF present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for VWF is added to the wells. After washing, Streptavidin 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 VWF bound in the initial step. The color development is stopped and the intensity of the color is measured.<br><br>Intended Uses: For the quantitative detection of Canine Von Willebrand Factor (VWF) concentration in serum, plasma and other biological fluids.
⇄⧉search_terms => string (592) "aaa13295 canine this assay has high sensitivity and excellent specificity fo...
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aaa13295 canine this assay has high sensitivity and excellent specificity for detection of prog no significant cross reactivity or interference between analogues was observed elisa kit von willebrand factor vwf f8vwf vwd coagulation viii 309,719 da 50950127 np_001002932.1 q28295 nm_001002932.1 q28311 q9tsi4 samples serum plasma other biological fluids type quantitative competitive range 0.15 ng ml 70 mean 6 independent assays intra precision within an three known concentration were tested twenty times on one plate to assess cv<8 inter in forty separate cv = sd meanx100 cv<12 ml70 mean6
⇄⧉specificity => string (192) "The Human ADAMTS13 ELISA Kit allows for the detection and quantification of ...
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The Human ADAMTS13 ELISA Kit allows for the detection and quantification of endogenous levels of natural and/or recombinant Human ADAMTS13 proteins within the range of 780 pg/ml - 50000 pg/ml.
⇄purity => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄⧉storage_stability => string (107) "Shipped and store at 4 degree C for 6 months, store at -20 degree C for one ...
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Shipped and store at 4 degree C for 6 months, store at -20 degree C for one year. Avoid freeze/thaw cycles.
⇄⧉products_name_syn => string (179) "C9orf8; A disintegrin and metalloproteinase with thrombospondin motifs 13; A...
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C9orf8; A disintegrin and metalloproteinase with thrombospondin motifs 13; ADAM-TS 13; ADAM-TS13; ADAMTS-13; von Willebrand factor-cleaving protease; vWF-CP; vWF-cleaving protease
⇄products_gene_name => string (8) "ADAMTS13"
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⇄⧉products_description => string (1511) "Principle of the Assay: The Human ADAMTS13 ELISA (Enzyme-Linked Immunosorben...
$value[5]['_source']['products_description']
Principle of the Assay: The Human ADAMTS13 ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of Human ADAMTS13 in Cell Culture Supernates, Serum, Plasma. This assay employs an antibody specific for Human ADAMTS13 coated on a 96-well plate. Standards and samples are pipetted into the wells and ADAMTS13 present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-Human ADAMTS13 antibody is added. After washing away unbound biotinylated antibody, HRP-conjugated streptavidin is pipetted to the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of ADAMTS13 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.<br><br>Background/Introduction: ADAMTS13 is a zinc-containing metalloprotease enzyme. The ADAMTS13 gene is mapped to chromosome 9q34 by genomic sequence analysis. It is reported that a metal-containing proteolytic enzyme (metalloprotease) in normal plasma cleaves the peptide bond between tyrosine at position 842 and methionine at position 843 in monomeric subunits of von Willebrand factor, thereby degrading the large multimers. And it is confirmed that the ADAMTS13 gene encodes the von Willebrand factor-cleaving protease (VWFCP). ADAMTS13 is secreted in blood and degrades large vWf multimers, decreasing their activity.
Defective B3GALTL Causes Peters-plus Syndrome (PpS) Pathway||1383054!!Disease Pathway||1268854!!Diseases Associated With O-glycosylation Of Proteins Pathway||1383049!!Diseases Of Glycosylation Pathway||1269010!!Metabolism Of Proteins Pathway||1268677!!O-glycosylation Of TSR Domain-containing Proteins Pathway||1268735!!O-linked Glycosylation Pathway||1268734!!Post-translational Protein Modification Pathway||1268701
⇄sp_protein_name => string (65) "A disintegrin and metalloproteinase with thrombospondin motifs 13"
⇄⧉search_terms => string (627) "aaa27868 human the adamts13 elisa kit allows for detection and quantificatio...
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aaa27868 human the adamts13 elisa kit allows for detection and quantification of endogenous levels natural or recombinant proteins within range 780 pg ml 50000 typical testing data standard curve reference only aaa27868_sc c9orf8 a disintegrin metalloproteinase with thrombospondin motifs 13 adam ts ts13 adamts von willebrand factor cleaving protease vwf cp isoform 1 preproprotein metallopeptidase type motif vwfcp 39,864 da ats13_human 21265034 np_620594.1 q76lx8 nm_139025.4 q6uy16 q710f6 q711t8 q96l37 q9h0g3 q9ugq1 ab069698 mrna samples cell culture supernates serum plasma sensitivity < 20 range780 motifs13 isoform1 <20
⇄⧉products_description => string (825) "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-Mouse vWF 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 (446) "aaa12425 mouse no cross reaction with other factors typical testing data sta...
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aaa12425 mouse no cross reaction with other factors typical testing data standard curve for reference only aaa12425_td elisa kit von willebrand factor vwf preproprotein vwd f8vwf coagulation viii 309,265 da antigen ii vwf_human 89191868 np_000543.2 p04275 nm_000552.3 q99806 gene 613554 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 range10
⇄⧉specificity => string (175) "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 rat vWF. No significant cross-reactivity or interference between rat vWF 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.
Rat von Willebrand Factor; vWF ELISA Kit; F8VWF; VWD; coagulation factor VIII VWF; von Willebrand factor
⇄products_gene_name => string (3) "VWF"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (727) "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 vWF has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any vWF present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for vWF 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 vWF bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (574) "aaa15467 rat this assay has high sensitivity and excellent specificity for d...
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aaa15467 rat this assay has high sensitivity and excellent specificity for detection of vwf no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15467_td elisa kit von willebrand factor f8vwf vwd coagulation viii 48,139 da vwf_rat 56404678 q62935.2 q62935 q78e31 q9z0p2 samples serum plasma tissue homogenates type sandwich quantitative range 0.312 ng ml 20 0.078 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in ml20
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||25-1600ng/ml!!Sensitivity||12.73ng/ml
⇄⧉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%
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⇄products_name => string (76) "A Disintegrin and Metalloproteinase with Thrombospondin Motifs 13 (ADAMTS13)"
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⇄⧉products_name_oem => string (92) "Human A Disintegrin and Metalloproteinase with Thrombospondin Motifs 13 (ADA...
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Human A Disintegrin and Metalloproteinase with Thrombospondin Motifs 13 (ADAMTS13) ELISA Kit
⇄products_name_syn => string (3) "N/A"
$value[8]['_source']['products_name_syn']
⇄products_gene_name => string (8) "ADAMTS13"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (960) "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 ADAMTS13 antibody. ADAMTS13 present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Human ADAMTS13 Antibody is added and binds to ADAMTS13 in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated ADAMTS13 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 ADAMTS13. 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 A Disintegrin and Metalloproteinase with Thrombospondin Motifs 13 (also known as ADAMTS13) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
Defective B3GALTL Causes Peters-plus Syndrome (PpS) Pathway||1383054!!Disease Pathway||1268854!!Diseases Associated With O-glycosylation Of Proteins Pathway||1383049!!Diseases Of Glycosylation Pathway||1269010!!Metabolism Of Proteins Pathway||1268677!!O-glycosylation Of TSR Domain-containing Proteins Pathway||1268735!!O-linked Glycosylation Pathway||1268734!!Post-translational Protein Modification Pathway||1268701
⇄sp_protein_name => string (65) "A disintegrin and metalloproteinase with thrombospondin motifs 13"
⇄⧉search_terms => string (717) "aaa11339 human typical testing data standard curve for reference only aaa113...
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aaa11339 human typical testing data standard curve for reference only aaa11339_sc elisa kit a disintegrin and metalloproteinase with thrombospondin motifs 13 adamts13 isoform 1 preproprotein adam metallopeptidase type motif vwfcp c9orf8 vwf cp ts13 adamts 147,804 da von willebrand factor cleaving protease ts 21265034 np_620594.1 q76lx8 nm_139025.4 q6uy16 q710f6 q711t8 q96l37 q9h0g3 q9ugq1 samples serum plasma cell culture supernates lysates tissue homogenates assay quantitative sandwich detection range 0.5ng ml 200ng sensitivity 0.36ng 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 motifs13 isoform1 x100
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of v...
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This assay has high sensitivity and excellent specificity for detection of vWF. No significant cross-reactivity or interference between vWF and analogues was observed.
⇄purity => string (3) "N/A"
$value[9]['_source']['purity']
⇄form => string (3) "N/A"
$value[9]['_source']['form']
⇄concentration => string (3) "N/A"
$value[9]['_source']['concentration']
⇄⧉storage_stability => string (475) "The stability of kit is determined by the loss rate of activity. The loss ra...
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The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. <br>To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
⇄⧉etc_term2 => string (412) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 ...
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Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level vWF were tested 20 times on one plate, respectively. Intra-Assay: CV<10%!!Inter-assay Precision||Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level vWF were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄products_name_syn => string (36) "F8VWF; VWD; von Willebrand antigen 2"
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⇄products_gene_name => string (3) "vWF"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (891) "Principle of the Assay: This assay employs the competitive inhibition enzyme...
$value[9]['_source']['products_description']
Principle of the Assay: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to vWF has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled vWF and unlabeled vWF (Standards or samples) with the pre-coated antibody specific to vWF. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of vWF in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of vWF in the sample.<br><br>Intended Uses: The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of vWF in canine plasma.
⇄⧉search_terms => string (633) "aaa20619 canine this assay has high sensitivity and excellent specificity fo...
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aaa20619 canine this assay has high sensitivity and excellent specificity for detection of vwf no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa20619_sc elisa kit von willebrand factor f8vwf vwd antigen 2 preproprotein 38,745 da 2alternative name s ii vwf_human 89191868 np_000543.2 p04275 nm_000552.3 q8tce8 q99806 193400 signal transduction hematology samples plasma type quantitative competitive range 9.88 800ng ml < 3.84ng intra precision within an 3 with low middle level were tested 20 times on one plate respectively cv antigen2 an3 tested20
⇄⧉specificity => string (189) "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 mouse ADAMTS13. No significant cross-reactivity or interference between mouse ADAMTS13 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[10]['_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 (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.
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⇄products_name => string (58) "ADAM metallopeptidase with thrombospondin type 1 motif, 13"
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⇄⧉products_name_oem => string (84) "Mouse ADAM metallopeptidase with thrombospondin type 1 motif, 13, ADAMTS13 E...
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Mouse ADAM metallopeptidase with thrombospondin type 1 motif, 13, ADAMTS13 ELISA Kit
⇄⧉products_name_syn => string (347) "Mouse ADAM metallopeptidase with thrombospondin type 1 motif; 13 (ADAMTS13) ...
$value[10]['_source']['products_name_syn']
Mouse ADAM metallopeptidase with thrombospondin type 1 motif; 13 (ADAMTS13) ELISA kit; C9orf8; DKFZp434C2322; FLJ42993; MGC118899; MGC118900; TTP; VWFCP; vWF-CP; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif; 13; vWF-cleaving protease; von Wil; ADAM metallopeptidase with thrombospondin type 1 motif; 13
⇄products_gene_name => string (8) "ADAMTS13"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (747) "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 ADAMTS13 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any ADAMTS13 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for ADAMTS13 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 ADAMTS13 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉ncbi_protein_info => string (272) "A disintegrin and metalloproteinase with thrombospondin motifs 13; vWF-cleav...
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A disintegrin and metalloproteinase with thrombospondin motifs 13; vWF-cleaving protease; von Willebrand factor-cleaving protease; vWF-CP mRNA for von Willebrand factor-cleaving; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 13
⇄ncbi_chrom_loc => string (3) "N/A"
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⇄ncbi_gene_id => string (6) "279028"
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⇄ncbi_mol_weight => string (10) "155,357 Da"
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⇄ncbi_pathways => string (3) "N/A"
$value[10]['_source']['ncbi_pathways']
⇄sp_protein_name => string (65) "A disintegrin and metalloproteinase with thrombospondin motifs 13"
⇄⧉search_terms => string (844) "aaa18019 mouse this assay has high sensitivity and excellent specificity for...
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aaa18019 mouse this assay has high sensitivity and excellent specificity for detection of adamts13 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18019_td elisa kit adam metallopeptidase with thrombospondin type 1 motif 13 c9orf8 dkfzp434c2322 flj42993 mgc118899 mgc118900 ttp vwfcp vwf cp a disintegrin like metalloprotease reprolysin cleaving protease von wil metalloproteinase motifs isoform gm710 ts13 adamts willebrand factor mrna 155,357 da ts ats13_mouse 47604978 np_001001322.1 q769j6 nm_001001322.2 q76lw1 a2alb4 samples serum plasma tissue homogenates quantitative sandwich range 78 pg ml 5000 < 19.5 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in type1 motif13 range78
⇄⧉specificity => string (181) "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 VWF. No significant cross-reactivity or interference between rabbit VWF 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_name_syn => string (71) "Rabbit von Willebrand Factor; VWF ELISA Kit; von Willebrand Factor; VWF"
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⇄products_gene_name => string (3) "VWF"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (727) "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 VWF has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any VWF present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for VWF 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 VWF bound in the initial step. The color development is stopped and the intensity of the color is measured.
Blood Clotting Cascade Pathway||198388!!Complement And Coagulation Cascades Pathway||198335!!Complement And Coagulation Cascades Pathway||83270!!Complement And Coagulation Cascades Pathway||484!!ECM-receptor Interaction Pathway||83265!!ECM-receptor Interaction Pathway||479!!Focal Adhesion Pathway||198353!!Focal Adhesion Pathway||83264!!Focal Adhesion Pathway||478!!Formation Of Fibrin Clot (Clotting Cascade) Pathway||1001318
⇄sp_protein_name => string (3) "VWF"
$value[11]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (3) "VWF"
$value[11]['_source']['sp_protein_name_syn']
⇄sp_gene_name => string (3) "Vwf"
$value[11]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (3) "N/A"
$value[11]['_source']['sp_gene_name_syn']
⇄sp_entry_name => string (12) "Q2I0J7_MOUSE"
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⇄sp_mim => string (3) "N/A"
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⇄⧉search_terms => string (585) "aaa15560 rabbit this assay has high sensitivity and excellent specificity fo...
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aaa15560 rabbit this assay has high sensitivity and excellent specificity for detection of vwf no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15560_td elisa kit von willebrand factor homolog vwd f8vwf ai551257 c630030d09 6820430p06rik b130011o06rik 309,102 da q2i0j7_mouse 86129842 abc86573.1 q8ciz8 q2i0j7 samples serum plasma type sandwich range 0.312 ng ml 20 0.078 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in ml20
⇄⧉specificity => string (373) "This assay has high sensitivity and excellent specificity for detection of v...
$value[12]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of vWF. No significant cross-reactivity or interference between vWF and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between vWF and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[12]['_source']['purity']
⇄form => string (3) "N/A"
$value[12]['_source']['form']
⇄concentration => string (3) "N/A"
$value[12]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄products_name_oem => string (39) "Porcine Von Willebrand Factor ELISA Kit"
$value[12]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[12]['_source']['products_name_syn']
⇄products_gene_name => string (3) "Vwf"
$value[12]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[12]['_source']['products_gene_name_syn']
⇄⧉products_description => string (1372) "Intended Uses: This vWF ELISA kit is a 1.5 hour solid-phase ELISA designed f...
$value[12]['_source']['products_description']
Intended Uses: This vWF ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Porcine vWF. This ELISA kit for research use only, not for therapeutic or test applications!<br><br>Principle of the Assay: vWF ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-vWF antibody and an vWF-HRP conjugate. The assay sample and buffer are incubated together with vWF-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 vWF concentration since vWF from samples and vWF-HRP conjugate compete for the anti-vWF antibody binding site. Since the number of sites is limited, as more sites are occupied by vWF from the sample, fewer sites are left to bind vWF-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The vWF concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (704) "aaa17010 porcine this assay has high sensitivity and excellent specificity f...
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aaa17010 porcine this assay has high sensitivity and excellent specificity for detection of vwf 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 aaa17010_sc elisa kit von willebrand factor homolog vwd f8vwf ai551257 c630030d09 6820430p06rik b130011o06rik 44,467 da antigen ii vwf_mouse 86129842 abc86573.1 q8ciz8 q60863 q6xuv6 q8biu9 q8cgn0 q9jk16 cardiovascular samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||0.3-80ng/mL!!Sensitivity||0.153ng/mL
⇄⧉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 (881) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[13]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Mouse vWF antibody. vWF present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Mouse vWF Antibody is added and binds to vWF in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated vWF 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 Mouse vWF. 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 Mouse von Willebrand Factor (also known as vWF) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉search_terms => string (546) "aaa11124 mouse typical testing data standard curve for reference only aaa111...
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aaa11124 mouse typical testing data standard curve for reference only aaa11124_sc elisa kit von willebrand factor vwf vwd f8vwf 38,745 da antigen 2alternative name s ii 340356 aab59458.1 p04275 q8tce8 q99806 samples serum plasma cell culture supernates ascites tissue homogenates or other biological fluids assay type quantitative sandwich detection range 0.3 80ng ml sensitivity 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 range0.3 x100
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||0.1-40ng/mL!!Sensitivity||0.054ng/mL
⇄⧉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 (873) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[14]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Rat vWF antibody. vWF present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Rat vWF Antibody is added and binds to vWF in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated vWF 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 Rat vWF. 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 Rat von Willebrand Factor (also known as vWF) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉search_terms => string (552) "aaa11261 rat typical testing data standard curve for reference only aaa11261...
$value[14]['_source']['search_terms']
aaa11261 rat typical testing data standard curve for reference only aaa11261_sc elisa kit von willebrand factor vwf vwd f8vwf 38,745 da antigen 2alternative name s ii 340356 aab59458.1 p04275 q8tce8 q99806 samples serum plasma cell culture supernates ascites tissue homogenates or other biological fluids assay type quantitative sandwich detection range 0.1 40ng ml sensitivity 0.054ng 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 range0.1 x100
⇄⧉specificity => string (373) "This assay has high sensitivity and excellent specificity for detection of v...
$value[15]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of vWF. No significant cross-reactivity or interference between vWF and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between vWF and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[15]['_source']['purity']
⇄form => string (3) "N/A"
$value[15]['_source']['form']
⇄concentration => string (3) "N/A"
$value[15]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄products_name_oem => string (37) "Sheep Von Willebrand Factor ELISA Kit"
$value[15]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[15]['_source']['products_name_syn']
⇄products_gene_name => string (3) "Vwf"
$value[15]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[15]['_source']['products_gene_name_syn']
⇄⧉products_description => string (1370) "Intended Uses: This vWF ELISA kit is a 1.5 hour solid-phase ELISA designed f...
$value[15]['_source']['products_description']
Intended Uses: This vWF ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Sheep vWF. This ELISA kit for research use only, not for therapeutic or test applications!<br><br>Principle of the Assay: vWF ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-vWF antibody and an vWF-HRP conjugate. The assay sample and buffer are incubated together with vWF-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 vWF concentration since vWF from samples and vWF-HRP conjugate compete for the anti-vWF antibody binding site. Since the number of sites is limited, as more sites are occupied by vWF from the sample, fewer sites are left to bind vWF-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The vWF concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (702) "aaa16909 sheep this assay has high sensitivity and excellent specificity for...
$value[15]['_source']['search_terms']
aaa16909 sheep this assay has high sensitivity and excellent specificity for detection of vwf 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 aaa16909_sc elisa kit von willebrand factor homolog vwd f8vwf ai551257 c630030d09 6820430p06rik b130011o06rik 44,467 da antigen ii vwf_mouse 86129842 abc86573.1 q8ciz8 q60863 q6xuv6 q8biu9 q8cgn0 q9jk16 cardiovascular samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of v...
$value[16]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of vWF. No significant cross-reactivity or interference between vWF 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 (475) "The stability of kit is determined by the loss rate of activity. The loss ra...
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The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. <br>To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
⇄⧉etc_term2 => string (412) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 ...
$value[16]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level vWF were tested 20 times on one plate, respectively. Intra-Assay: CV<10%!!Inter-assay Precision||Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level vWF were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄products_name_syn => string (36) "F8VWF; VWD; von Willebrand antigen 2"
$value[16]['_source']['products_name_syn']
⇄products_gene_name => string (3) "vWF"
$value[16]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[16]['_source']['products_gene_name_syn']
⇄⧉products_description => string (892) "Principle of the Assay: This assay employs the competitive inhibition enzyme...
$value[16]['_source']['products_description']
Principle of the Assay: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to vWF has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled vWF and unlabeled vWF (Standards or samples) with the pre-coated antibody specific to vWF. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of vWF in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of vWF in the sample.<br><br>Intended Uses: The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of vWF in porcine plasma.
⇄⧉search_terms => string (637) "aaa20675 porcine this assay has high sensitivity and excellent specificity f...
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aaa20675 porcine this assay has high sensitivity and excellent specificity for detection of vwf no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa20675_sc elisa kit von willebrand factor f8vwf vwd antigen 2 preproprotein 38,745 da 2alternative name s ii vwf_human 89191868 np_000543.2 p04275 nm_000552.3 q8tce8 q99806 193400 signal transduction hematology samples plasma type quantitative competitive range 12.35 1,000ng ml < 4.62ng intra precision within an 3 with low middle level were tested 20 times on one plate respectively cv antigen2 an3 tested20
<b>Storage:</b><br>Avoid repeated freeze/thaw cycles.<br>Store at 4 degree C for frequent use.<br>Aliquot and store at -20 degree C for 24 months.<br><br><b>Stability Test:</b><br>thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 degree C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
Western blotting: 0.5-2ug/mL<br>Immunohistochemistry: 5-20ug/mL<br>Immunocytochemistry: 5-20ug/mL<br>Optimal working dilutions must be determined by end user.
aaa20193 rabbit mus musculus mouse polyclonal antigen specific affinity chromatography followed by protein a supplied as solution form in 0.01m pbs ph7.4 containing 0.05 proclin 300 50 glycerol western blot wb immunohistochemistry ihc immunocytochemistry icc immunoprecipitation ip blotting 0.5 2ug ml 5 20ug optimal working dilutions must be determined end user sample recombinant vwf aaa20193_wb dab staining on p samples testis tissue primary ab anti antibody second hrp linked caprine igg catalog mbs2086047 aaa20193_ihc2 stomach aaa20193_ihc5 von willebrand factor to vwd f8vwf ai551257 c630030d09 6820430p06rik b130011o06rik 2alternative name s ii 115511022 np_035838.3 q8ciz8 nm_011708.4 q60863 q6xuv6 q8biu9 q8cgn0 q9jk16 source preparation traits liquid cross reactivity rat immunogen asp1498~val1665 expressed e.coli mbs2010236 proclin300 blotting0.5 ml5
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of v...
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This assay has high sensitivity and excellent specificity for detection of vWFAg. No significant cross-reactivity or interference between vWFAg and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between vWFAg 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[18]['_source']['form']
⇄concentration => string (3) "N/A"
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⇄storage_stability => string (34) "Store all reagents at 2-8 degree C"
⇄⧉products_name_syn => string (149) "Human von Willebrand Factor antigen, vWF:Ag ELISA Kit; von Willebrand Factor...
$value[18]['_source']['products_name_syn']
Human von Willebrand Factor antigen, vWF:Ag ELISA Kit; von Willebrand Factor antigen, vWF:Ag; von Willebrand Factor antigen, vWF:Ag ELISA Kit (Human)
⇄products_gene_name => string (3) "VWF"
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⇄products_gene_name_syn => string (3) "N/A"
$value[18]['_source']['products_gene_name_syn']
⇄⧉products_description => string (1402) "Principle of the Assay: vWFAg ELISA kit applies the competitive enzyme immun...
$value[18]['_source']['products_description']
Principle of the Assay: vWFAg ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-vWFAg antibody and an vWFAg-HRP conjugate. The assay sample and buffer are incubated together with vWFAg-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 vWFAg concentration since vWFAg from samples and vWFAg-HRP conjugate compete for the anti-vWFAg antibody binding site. Since the number of sites is limited, as more sites are occupied by vWFAg from the sample, fewer sites are left to bind vWFAg-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The vWFAg concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This vWFAg ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human vWFAg. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Blood Clotting Cascade Pathway||198388!!Complement And Coagulation Cascades Pathway||198335!!Complement And Coagulation Cascades Pathway||83270!!Complement And Coagulation Cascades Pathway||484!!ECM-receptor Interaction Pathway||83265!!ECM-receptor Interaction Pathway||479!!Focal Adhesion Pathway||198353!!Focal Adhesion Pathway||83264!!Focal Adhesion Pathway||478!!Formation Of Platelet Plug Pathway||366293
⇄sp_protein_name => string (3) "VWF"
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⇄sp_protein_name_syn => string (3) "N/A"
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⇄sp_gene_name => string (3) "Vwf"
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⇄sp_gene_name_syn => string (3) "N/A"
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⇄sp_entry_name => string (12) "Q2I0J7_MOUSE"
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⇄sp_mim => string (3) "N/A"
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⇄sp_interactions => string (3) "N/A"
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⇄products_url => string (3) "N/A"
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⇄products_viewed => string (1) "0"
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⇄⧉search_terms => string (713) "aaa16645 human this assay has high sensitivity and excellent specificity for...
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aaa16645 human this assay has high sensitivity and excellent specificity for detection of vwf ag 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 aaa16645_sc elisa kit von willebrand factor antigen vwf:ag homolog vwd f8vwf ai551257 c630030d09 6820430p06rik b130011o06rik ottmusp00000025031 309,102 da q2i0j7_mouse 86129842 q2i0j7 q2i0j8 q3td35 q3tpe1 q3u017 q8ciz8 q9wuq6 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
<b>Storage:</b><br>Avoid repeated freeze/thaw cycles.<br>Store at 4 degree C for frequent use.<br>Aliquot and store at -20 degree C for 24 months.<br><br><b>Stability Test:</b><br>thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 degree C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
Western blotting: 0.5-2ug/mL<br>Immunohistochemistry: 5-20ug/mL<br>Immunocytochemistry: 5-20ug/mL<br>Optimal working dilutions must be determined by end user.
⇄⧉testing_protocols => string (646) "IHC (Immunohistchemistry)||DAB staining on IHC-P;<br>Samples: Rat Pancreas T...
$value[19]['_source']['testing_protocols']
IHC (Immunohistchemistry)||DAB staining on IHC-P;<br>Samples: Rat Pancreas Tissue;<br>Primary Ab: 10ug/ml Rabbit Anti-Rat vWF Antibody<br>Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody(Immunohistochemistry)||DAB staining on IHC-P;<br>Samples: Rat Pancreas Tissue||AAA20090_IHC5.jpg!!WB (Western Blot)||Western Blot;<br>Sample: Rat Plasma<br>Primary Ab: 2ug/ml Rabbit Anti-Rat vWF Antibody<br>Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody (Western Blot)||Western Blot:<br>Sample: Recombinant vWF, Rat.||AAA20090_WB2.jpg!!WB (Western Blot)||Western Blot:<br>Sample: Rat Serum.||AAA20090_WB.jpg
⇄⧉search_terms => string (979) "aaa20090 rabbit rat polyclonal affinity chromatography supplied as solution ...
$value[19]['_source']['search_terms']
aaa20090 rabbit rat polyclonal affinity chromatography supplied as solution form in pbs ph7.4 containing 0.02 nan3,50 glycerol the antibody is a raised against vwf it has been selected for its ability to recognize immunohistochemical staining andwestern blotting immunocytochemistry icc immunohistochemistry ihc formalin paraffin elisa eia western blot wb 1:100 400 fixed cells 500 frozen section 1:50 200 enzyme linked immunosorbent assay sample serum aaa20090_wb recombinant aaa20090_wb2 dab on p samples pancreas tissue aaa20090_ihc aaa20090_ihc2 antigen target protein fused with n terminal his tag and sequence listed below mghhhhhhsg sef sl vldvvfvlea sdevgeanfn kskefleevi qrmdvspagt hiavlqysyt vnveytfkea qskedvlrhv reiryqggnr tntgqalqyl sehsfsp von willebrand factor 48,139 da 56404678 q62935.2 q62935 q78e31 q9z0p2 immunogen ser269~pro367 expressed e.coli cross reactivity conjugated apc version of this item also available catalog #mbs2048301 1:100400 cells500 1:50200
