FGF-2 Polyclonal Antibody
¥680.00
ROR2 (Phospho Ser449) rabbit pAb
活动价：
¥680.00
市场价：¥880.00
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产品规格：
- 50μL
- 100μL
货号：
FAB2612446
- 产品信息
商品描述
靶点-Target
ROR2
反应性
Human,Mouse,Rat
应用
WB
宿主物种-Host Species
Rabbit
同种型-Isotype
IgG
修饰-Modification
Phospho
MW(Calculated)
104kD
推荐稀释比
WB 1:500-2000
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 serum by affinity-chromatography using 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 human ROR2 (Phospho-Ser449)
特异性
This antibody detects endogenous levels of ROR2 (Phospho-Ser449) at Human, Mouse,Rat
基因名称
ROR2 NTRKR2
蛋白名称
ROR2 (Phospho-Ser449)
别名
Tyrosine-protein kinase transmembrane receptor ROR2;Neurotrophic tyrosine kinase, receptor-related 2;
Organism-1
Human
基因ID-1
4920
SwissProt-1
Q01974
Organism-2
Mouse
SwissProt-2
Q9Z138
背景
The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008],
细胞定位
Cell membrane ; Single-pass type I membrane protein .
