- 靶点:
- Ephrin-B1
- 简介:
- >>Axon guidance
- 基因名称:
- EFNB1
- 蛋白名称:
- Ephrin-B1
- Human Gene Id:
- 1947
- Human Swiss Prot No:
- P98172
- Mouse Gene Id:
- 13641
- Mouse Swiss Prot No:
- P52795
- Rat Swiss Prot No:
- 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.
- 组成:
- Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
- 来源:
- Polyclonal, Rabbit,IgG
- 稀释:
- WB 1:500 - 1:2000. ELISA: 1:40000. Not yet tested in other applications.
- 纯化工艺:
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
- 浓度:
- 1 mg/ml
- 储存:
- -15°C to -25°C/1 year(Do not lower than -25°C)
- 其他名称:
- EFNB1;EFL3;EPLG2;LERK2;Ephrin-B1;EFL-3;ELK ligand;ELK-L;EPH-related receptor tyrosine kinase ligand 2;LERK-2
- 实测条带:
- 38kD
- 背景:
- 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],
- 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.,
- 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. .
- 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).
Activation of ephrinb1/EPHB2/MAP-2/NMDAR Mediates Hippocampal Neurogenesis Promoted by Transcranial Direct Current Stimulation in Cerebral-Ischemic Mice. NEUROMOLECULAR MEDICINE Neuromol Med. 2021 Dec;23(4):521-530 WB Mouse 1 : 1000 Hippocampal
货号:YT1594
Fatty acid synthase affects expression of ErbB receptors in epithelial to mesenchymal transition of breast cancer cells and invasive ductal carcinoma. Oncology Letters Oncol Lett. 2017 Nov;14(5):5934-5946 WB,IHC Human 1:200,1:200,1:200 MCF-7 cell
货号:YT1594
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- Antibody-FAQs
- 产品图片
- Western Blot analysis of various cells using Ephrin-B1 Polyclonal Antibody
- Western blot analysis of lysates from COS7 cells, using EFNB1 Antibody. The lane on the right is blocked with the synthesized peptide.