Cn|En

现货抗体产品库

Met (Phospho Tyr1235) Rabbit Polyclonal Antibody

产品详情 相关文献 产品问答 相关产品

产品基本信息

产品货号
BD-PP1587
产品名称
Met (Phospho Tyr1235) Rabbit Polyclonal Antibody
别名
Hepatocyte growth factor receptor (HGF receptor;EC 2.7.10.1;HGF/SF receptor;Proto-oncogene c-Met;Scatter factor receptor;SF receptor;Tyrosine-protein kinase Met)
类别
常规抗体
基因名称
MET
蛋白名称
Met (Phospho Tyr1235)
推荐应用
WB
反应种属
Human,Mouse,Rat
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
4233
Human Gene Link
https://www.uniprot.org/uniprot/4233
Human Swissprot No.
P08581
Human Swissprot Link
https://www.uniprot.org/uniprotkb/P08581/entry
Mouse Gene Link
https://www.uniprot.org/uniprot/0
Mouse Swissprot No.
P16056
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/P16056
Rat Gene ID
24553
Rat Gene Link
https://www.uniprot.org/uniprot/24553
Rat Swissprot No.
P97523
Rat Swissprot Link
https://www.uniprot.org/uniprotkb/P97523
免疫原
Synthesized peptide derived from human Met (Phospho Tyr1235)
特异性
This antibody detects endogenous levels of Human,Mouse,Rat Met (Phospho Tyr1235)
稀释度
WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
预测分子量
140170kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
catalytic activity:ATP + a [protein]-L-tyrosine = ADP + a [protein]-L-tyrosine phosphate.,disease:Activation of MET after rearrangement with the TPR gene produces an oncogenic protein.,disease:Defects in MET are a cause of hepatocellular carcinoma (HCC) [MIM:114550].,disease:Defects in MET are a cause of hereditary papillary renal carcinoma (HPRC) [MIM:605074]; also known as papillary renal cell carcinoma 2 (RCCP2). HPRC is a form of inherited kidney cancer characterized by a predisposition to develop multiple, bilateral papillary renal tumors. The pattern of inheritance is consistent with autosomal dominant transmission with reduced penetrance.,disease:Defects in MET may be associated with gastric cancer.,disease:Genetic variations in MET may be associated with susceptibility to autism type 9 (AUTS9) [MIM:611015]. Autism is a neurodevelopmental disorder characterized by disturbance in language, perception and socialization. The disorder is classically defined by a triad of limited or absent verbal communication, a lack of reciprocal social interaction or responsiveness, and restricted, stereotypical, and ritualized patterns of interests and behavior.,domain:The kinase domain is involved in SPSB1 binding.,function:Receptor for hepatocyte growth factor and scatter factor. Has a tyrosine-protein kinase activity. Functions in cell proliferation, scattering, morphogenesis and survival.,online information:C-MET entry,similarity:Belongs to the protein kinase superfamily. Tyr protein kinase family.,similarity:Contains 1 protein kinase domain.,similarity:Contains 1 Sema domain.,similarity:Contains 3 IPT/TIG domains.,subunit:Heterodimer formed of an alpha chain (50 kDa) and a beta chain (145 kDa) which are disulfide linked. Binds PLXNB1 and GRB2. Interacts with SPSB1, SPSB2 and SPSB4 (By similarity). Interacts with INPP5D/SHIP1. When phosphorylated at Tyr-1356, interacts with INPPL1/SHIP2. Interacts with RANBP9 and RANBP10, as well as SPSB1, SPSB2, SPSB3 and SPSB4. SPSB1 binding occurs in the presence and in the absence of HGF, however HGF treatment has a positive effect on this interaction. Interacts with MUC20; prevents interaction with GRB2 and suppresses hepatocyte growth factor-induced cell proliferation.,
组织表达
Expressed in normal hepatocytes as well as in epithelial cells lining the stomach, the small and the large intestine. Found also in basal keratinocytes of esophagus and skin. High levels are found in liver, gastrointestinal tract, thyroid and kidney. Also present in the brain. Expressed in metaphyseal bone (at protein level) (PubMed:26637977).
细胞定位
Membrane; Single-pass type I membrane protein.; [Isoform 3]: Secreted.
功能
MAPKKK cascade,?activation of MAPK activity,?neuron migration,?protein amino acid phosphorylation,?phosphorus metabolic process,?phosphate metabolic process,?cell motion,?cell surface receptor linked signal transduction,?enzyme linked receptor protein signaling pathway,?transmembrane receptor protein tyrosine kinase signaling pathway,intracellular signaling cascade,?protein kinase cascade,?muscle organ development,?lactation,?behavior,?cell proliferation,?phosphorylation,?cell migration,?regulation of phosphate metabolic process,?sperm motility,?adult behavior,?mammary gland development,?multicellular organism reproduction,?positive regulation of kinase activity,regulation of phosphorylation,?positive regulation of catalytic activity,?regulation of MAP kinase activity,?positive regulation of MAP kinase activity,?regulation of kinase activity,?positive regulation of molecular function,?regulation of protein kinase activity,?positive regulation of protein kinase activity,?protein amino acid autophosphorylation,hepatocyte growth factor receptor signaling pathway,?reproductive process in a multicellular organism,?gland development,?cell motility,?regulation of phosphorus metabolic process,?regulation of transferase activity,?positive regulation of transferase activity,?myoblast proliferation,?localization of cell,
期货
现货
纯化
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

相关文献

产品问答

相关产品

免责声明| 法律支持| 联系方式

市场:027-65023363   行政/人事:027-62439686   邮箱:marketing@brainvta.com  

销售总监:张经理  18995532642  华东区:陈经理 18013970337   华南区:王经理 13100653525   华中/西区:杨经理 18186518905   华北区:张经理 18893721749

地址:中国武汉东湖高新区光谷七路128号中科开物产业园1号楼

Copyright © 武汉枢密脑科学技术有限公司. All RIGHTS RESERVED.
鄂ICP备2021009124号 DIGITAL BY VTHINK