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Ephrin-B1 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT1594
产品名称
Ephrin-B1 Rabbit Polyclonal Antibody
别名
EFNB1; EFL3; EPLG2; LERK2; Ephrin-B1; EFL-3; ELK ligand; ELK-L; EPH-related receptor tyrosine kinase ligand 2; LERK-2
类别
常规抗体
基因名称
EFNB1
蛋白名称
Ephrin-B1
推荐应用
WB
反应种属
Human,Mouse,Rat,Monkey
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
1947
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1947
Human Swissprot No.
P98172
Human Swissprot Link
http://www.uniprot.org/uniprotkb/P98172/entry
Mouse Gene ID
13641
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=13641
Mouse Swissprot No.
P52795
Mouse Swissprot Link
http://www.uniprot.org/uniprot/P52795
Rat Swissprot No.
P52796
Rat Swissprot Link
http://www.uniprot.org/uniprot/P52796
免疫原
The antiserum was produced against synthesized peptide derived from human EFNB1. AA range:283-332
特异性
Ephrin-B1 Polyclonal Antibody detects endogenous levels of Ephrin-B1 protein.
稀释度
WB 1:500 - 1:2000. ELISA: 1:40000. Not yet tested in other applications.
预测分子量
38kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
The protein encoded by this gene is a type I membrane protein and a ligand of Eph-related receptor tyrosine kinases. It may play a role in cell adhesion and function in the development or maintenance of the nervous system. [provided by RefSeq, Jul 2008],
组织表达
Widely expressed (PubMed:8070404, PubMed:7973638). Detected in both neuronal and non-neuronal tissues (PubMed:8070404, PubMed:7973638). Seems to have particularly strong expression in retina, sciatic nerve, heart and spinal cord (PubMed:7973638).
细胞定位
Cell membrane ; Single-pass type I membrane protein . Membrane raft . May recruit GRIP1 and GRIP2 to membrane raft domains. .; [Ephrin-B1 C-terminal fragment]: Cell membrane ; Single-pass type I membrane protein .; [Ephrin-B1 intracellular domain]: Nucleus . Colocalizes with ZHX2 in the nucleus. .
信号通路
Axon guidance;
功能
disease:Defects in EFNB1 are a cause of craniofrontonasal syndrome (CFNS) [MIM:304110]; also known as craniofrontonasal dysplasia (CFND). CFNS is an X-linked inherited syndrome characterized by hypertelorism, coronal synostosis with brachycephaly, downslanting palpebral fissures, clefting of the nasal tip, joint anomalies, longitudinally grooved fingernails and other digital anomalies.,function:Binds to the receptor tyrosine kinases EPHB1 and EPHA1. Binds to, and induce the collapse of, commissural axons/growth cones in vitro. May play a role in constraining the orientation of longitudinally projecting axons.,induction:By TNF-alpha.,PTM:Inducible phosphorylation of tyrosine residues in the cytoplasmic domain.,similarity:Belongs to the ephrin family.,subunit:Interacts with GRIP1 and GRIP2.,tissue specificity:Heart, placenta, lung, liver, skeletal muscle, kidney, pancreas.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Western blot analysis of lysates from COS7 cells, using EFNB1 Antibody. The lane on the right is blocked with the synthesized peptide.

Western Blot analysis of various cells using Ephrin-B1 Polyclonal Antibody

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