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货号:CSB-PA891951LA01HU
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规格:¥440
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促销:
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图片:
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) ADAMTS7 Polyclonal antibody
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Uniprot No.:Q9UKP4
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基因名:ADAMTS7
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别名: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
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宿主:Rabbit
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反应种属:Human, Mouse
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免疫原:Recombinant Human A disintegrin and metalloproteinase with thrombospondin motifs 7 protein (242-593AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,ADAMTS7 Antibody (CSB-PA891951LA01HU),的标记方式是Non-conjugated。对于ADAMTS7 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB, IHC
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:2000 IHC 1:20-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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.
引用文献
相关产品
靶点详情
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功能:Metalloprotease that may play a role in the degradation of COMP.
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基因功能参考文献:
- 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
- Multivariate analysis showed that DeltaADAMTS-7(day 7 minus day 1) was independently associated with left ventricular reverse remodeling PMID: 29523183
- Genetic variation at the ADAMTS7 locus is associated with reduced severity of coronary artery disease. PMID: 29089340
- 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
- The findings suggest that upregulation of ADAMTS-7 and down regulation of COMP are associated with human AA. PMID: 28849199
- The native overfunctional ADAMTS7 allele (A) may accelerate VSMC migration and lead to neointimal thickening, atherosclerosis progression and acute plaque events. PMID: 27614204
- miR-105/Runx2 axis mediates FGF2-induced ADAMTS expression in osteoarthritis cartilage. PMID: 26816250
- Allelic variation that associates with reduced ADAMTS7 expression confers stronger coronary heart disease protection in never-smokers than in ever-smokers. PMID: 28461624
- 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
- ADAMTS7 and LPA single nucleotide polymorphisms are related to a 24-h ambulatory systolic-diastolic pressure regression index. PMID: 28092973
- 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
- Our results indicate the presence of ADAMTS-7 in human NP cells and imply its potential role in disc degeneration. PMID: 26446668
- The main contribution of this study is the proposal of a pharmacophore for ADAMTS7. PMID: 26872430
- The significant associations observed between this coding variant in ADAMTS7 and the risk of CAD development. PMID: 26189211
- 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
- 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
- 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
- There was a reduction in the amount of cleaved ADAMTS7 prodomain in media conditioned by VSMCs of the G/G genotype. PMID: 23415669
- 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
- identified ADAMTS7 as novel locus for CAD and association of ABO with MI in the presence of CAD PMID: 21239051
- ADAMTS-7 is the first metalloproteinase found to bind directly to and degrade COMP PMID: 16585064
- ADAMTS-7 and ADAMTS-12 are newly identified enzymes responsible for cartilage oligomeric matrix protein degradation in arthritis. PMID: 19098927
- 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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亚细胞定位:Secreted, extracellular space, extracellular matrix.
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组织特异性:Expressed in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Detected in meniscus, bone, tendon, cartilage, synovium, fat and ligaments.
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数据库链接:
HGNC: 223
OMIM: 605009
KEGG: hsa:11173
STRING: 9606.ENSP00000373472
UniGene: Hs.16441
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