ADAMTS7 Antibody, Biotin conjugated

Code CSB-PA891951LD01HU
Size US$299
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Product Details

Full Product Name Rabbit anti-Homo sapiens (Human) ADAMTS7 Polyclonal antibody
Uniprot No. Q9UKP4
Target Names ADAMTS7
Alternative Names A disintegrin and metalloprotease with thrombospondin motifs 7 preproprotein antibody; A disintegrin and metalloproteinase with thrombospondin motifs 7 antibody; A disintegrin like and metalloprotease (reprolysin type) with thrombospondin type 1 motif 7 antibody; A disintegrin like and metalloprotease with thrombospondin type 1 motif 7 antibody; ADAM metallopeptidase with thrombospondin type 1 motif 7 antibody; ADAM metallopeptidase with thrombospondin type 1 motif 7 preproprotein antibody; ADAM TS 7 antibody; ADAM TS7 antibody; ADAM-TS 7 antibody; ADAM-TS7 antibody; ADAMTS 7 antibody; ADAMTS-7 antibody; Adamts7 antibody; ATS7_HUMAN antibody; COMPase antibody; DKFZp434H204 antibody
Raised in Rabbit
Species Reactivity Human
Immunogen Recombinant Human A disintegrin and metalloproteinase with thrombospondin motifs 7 protein (242-593AA)
Immunogen Species Homo sapiens (Human)
Conjugate Biotin
Clonality Polyclonal
Isotype IgG
Purification Method >95%, Protein G purified
Concentration It differs from different batches. Please contact us to confirm it.
Buffer Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Form Liquid
Tested Applications ELISA
Protocols ELISA Protocol
Troubleshooting and FAQs Antibody FAQs
Storage Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Data

Function Metalloprotease that may play a role in the degradation of COMP.
Gene References into Functions
  1. data show that ADAMTS-7 is associated with a vulnerable plaque phenotype in human carotid lesions. These data support previous observations of a potential proatherogenic role of ADAMTS-7. PMID: 28623250
  2. Multivariate analysis showed that DeltaADAMTS-7(day 7 minus day 1) was independently associated with left ventricular reverse remodeling PMID: 29523183
  3. Genetic variation at the ADAMTS7 locus is associated with reduced severity of coronary artery disease. PMID: 29089340
  4. Studied gene expression of genetic variants of ADAMTS7 in atherosclerotic occlusive peripheral arterial disease (PAD). Found mRNA levels of ADAMTS7 to be significantly higher in PAD patients than controls, and that the rs1994016 CC and rs3825807 TT genotypes may upregulate ADAMTS7 mRNA levels and may influence PAD development. PMID: 28205274
  5. The findings suggest that upregulation of ADAMTS-7 and down regulation of COMP are associated with human AA. PMID: 28849199
  6. The native overfunctional ADAMTS7 allele (A) may accelerate VSMC migration and lead to neointimal thickening, atherosclerosis progression and acute plaque events. PMID: 27614204
  7. miR-105/Runx2 axis mediates FGF2-induced ADAMTS expression in osteoarthritis cartilage. PMID: 26816250
  8. Allelic variation that associates with reduced ADAMTS7 expression confers stronger coronary heart disease protection in never-smokers than in ever-smokers. PMID: 28461624
  9. During inflammatory conditions, AP-1 and Sp1 sustained the expression of ADAMTS7, and ADAMTS7 sustained the expression of catabolic genes in nucleus pulposus cells PMID: 27516213
  10. ADAMTS7 and LPA single nucleotide polymorphisms are related to a 24-h ambulatory systolic-diastolic pressure regression index. PMID: 28092973
  11. Expression of miR-26a and miR-29a was significantly down regulated in leukoplakia and cancer tissues but up regulated in lichen planus tissues. Expression of target genes such as, ADAMTS7, ATP1B1, COL4A2, CPEB3, CDK6, DNMT3a and PI3KR1 was significantly down regulated in at least two of three disease types with respect to normal tissues. PMID: 27515006
  12. Our results indicate the presence of ADAMTS-7 in human NP cells and imply its potential role in disc degeneration. PMID: 26446668
  13. The main contribution of this study is the proposal of a pharmacophore for ADAMTS7. PMID: 26872430
  14. The significant associations observed between this coding variant in ADAMTS7 and the risk of CAD development. PMID: 26189211
  15. Logistic regression analysis indicated that the association between ADAMTS-7 and heart failure after AMI was independent from traditional cardiovascular risk factors and other biomarkers PMID: 25885961
  16. Data conclude that ADAMTS-7 level appears to be positively associated with expression of TNF-alpha and Phospho-NF-kappaB P65 in cartilage, which may imply its association with cartilage destruction of ONFH. PMID: 25653475
  17. ADAMTS7 localized to cells having smooth muscle cell markers in human coronary artery disease lesions. Cultured vascular smooth muscle cells had ADAMTS7 at the cytoplasm and cell membrane, where it colocalized with markers of podosomes. PMID: 25712206
  18. There was a reduction in the amount of cleaved ADAMTS7 prodomain in media conditioned by VSMCs of the G/G genotype. PMID: 23415669
  19. statistically significant increase in mRNA expression of ADAMTS-7 and ADAMTS-12 was observed in the endplate cells in degenerative discs compared with nondegenerative discs PMID: 22247065
  20. identified ADAMTS7 as novel locus for CAD and association of ABO with MI in the presence of CAD PMID: 21239051
  21. ADAMTS-7 is the first metalloproteinase found to bind directly to and degrade COMP PMID: 16585064
  22. ADAMTS-7 and ADAMTS-12 are newly identified enzymes responsible for cartilage oligomeric matrix protein degradation in arthritis. PMID: 19098927
  23. Findings demonstrate that ADAMTS-7, a direct target of PTHrP signaling, negatively regulates endochondral bone formation by associating with and inactivating GEP chondrogenic growth factor. PMID: 19487464

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Subcellular Location Secreted, extracellular space, extracellular matrix
Tissue Specificity Expressed in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Detected in meniscus, bone, tendon, cartilage, synovium, fat and ligaments.
Database Links

HGNC: 223

OMIM: 605009

KEGG: hsa:11173

STRING: 9606.ENSP00000373472

UniGene: Hs.16441

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