- 产品信息
商品描述
靶点-Target
ADAMTS-2
反应性
Human,Mouse
应用
WB,ELISA
宿主物种-Host Species
Rabbit
同种型-Isotype
IgG
修饰-Modification
Unmodified
MW(Observed)
100kD
推荐稀释比
WB 1:500-1:2000;ELISA 1:10000;Not yet tested in other applications.
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
克隆性
Polyclonal
免疫原
Synthesized peptide derived from ADAMTS-2 . at AA range: 1140-1220
特异性
ADAMTS-2 Polyclonal Antibody detects endogenous levels of ADAMTS-2 protein.
基因名称
ADAMTS2
蛋白名称
A disintegrin and metalloproteinase with thrombospondin motifs 2
别名
ADAMTS2;PCINP;PCPNI;A disintegrin and metalloproteinase with thrombospondin motifs 2;ADAM-TS 2;ADAM-TS2;ADAMTS-2;Procollagen I N-proteinase;PC I-NP;Procollagen I/II amino propeptide-processing enzyme;Procollagen N-endopeptidase;pNPI
Organism-1
Human
基因ID-1
9509
SwissProt-1
O95450
Organism-2
Mouse
SwissProt-2
Q8C9W3
背景
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically
细胞定位
Secreted, extracellular space, extracellular matrix .





