ADAMTS-17 Polyclonal Antibody
活动价:
市场价:¥880.00
- 50μL
- 100μL
FAB2612705
- 产品信息
商品描述
靶点-Target
ADAMTS-17
反应性
Human,Mouse
应用
IHC,IF,ELISA
宿主物种-Host Species
Rabbit
同种型-Isotype
IgG
修饰-Modification
Unmodified
MW(Calculated)
121kD
推荐稀释比
IHC 1:100-1:300;ELISA 1:20000;IF 1:50-200
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-17 . at AA range: 150-230
特异性
ADAMTS-17 Polyclonal Antibody detects endogenous levels of ADAMTS-17 protein.
基因名称
ADAMTS17
蛋白名称
A disintegrin and metalloproteinase with thrombospondin motifs 17
别名
ADAMTS17;A disintegrin and metalloproteinase with thrombospondin motifs 17;ADAM-TS 17;ADAM-TS17;ADAMTS-17
Organism-1
Human
基因ID-1
170691
SwissProt-1
Q8TE56
背景
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members 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 protein, which may promote breast cancer cell growth and survival. Mutations in this gene are associated with a Weill-Marchesani-like syndrome, which is characterized by lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. [provided by RefSeq, May 2016],
细胞定位
Secreted, extracellular space, extracellular matrix .





