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ROR2 (Phospho Ser449) rabbit pAb

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说明书下载
货号: PF0251
货期: 现货
价格: 50μL/960;100μL/1600;200μL/2560
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靶点: ROR2
应用: WB
反应性 : Human,Mouse,Rat
宿主物种 : Rabbit
MW(CalcμLated) : 104kD
同种型-Isotype : IgG

隐藏域元素占位

详细信息

修饰-Modification : Phospho
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

抗原&靶点信息

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 : ROR2;NTRKR2;Tyrosine-protein kinase transmembrane receptor ROR2;Neurotrophic tyrosine kinase;receptor-related 2

数据库链接:

Organism

基因 ID

SwissProt

Mouse
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 .

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