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所在位置:所有产品 > 抗体抗原 > 一抗 > FGFR2抗体
FGFR2抗体图片
产品货号:
Z38032
中文名称:
FGFR2抗体
英文名称:
Anti-FGFR2 Antibody
产品规格:
50μl|100μl|150μl
发货周期:
1~3天
产品价格:
询价
抗体名称Anti-FGFR2 Antibody
指标别名BEK;BFR 1;CD332;CEK3;CFD1;ECT1;FGFR 2;FGFR2;JWS;K SAM;KGFR;KSAM;TK14;TK25
克隆性Monoclonal
检验物种human,mouse,rat
应用范围WB,IP
基因名称FGFR2
抗体来源Rabbit
抗体类型IgG
免疫原A synthesized peptide derived from human FGFR2
实际分子量145KD
成分500μg/mL;Rabbit IgG in phosphate buffered saline,pH7.4,150mM NaCl,0.02% sodium azide and 50% glycerol.
纯化方式Affinity-chromatography
浓度500μg/mL
产品形态溶液
保存条件12 months from date of receipt,-20℃ as supplied.6 months 2 to 8℃ after reconstitution.Avoid repeated freezing and thawing.
背景资料The protein encoded by this gene is a member of the fibroblast growth factor receptor family,where amino acid sequence is highly conserved between members and throughout evolution.FGFR family members differ from one another in their ligand affinities and tissue distribution.A full-length representative protein consists of an extracellular region,composed of three immunoglobulin-like domains,a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain.The extracellular portion of the protein interacts with fibroblast growth factors,setting in motion a cascade of downstream signals,ultimately influencing mitogenesis and differentiation.This particular family member is a high-affinity receptor for acidic,basic and/or keratinocyte growth factor,depending on the isoform.Mutations in this gene are associated with Crouzon syndrome,Pfeiffer syndrome,Craniosynostosis,Apert syndrome,Jackson-Weiss syndrome,Beare-Stevenson cutis gyrata syndrome,Saethre-Chotzen syndrome,and syndromic craniosynostosis.Multiple alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
Uniprot IDP21802
基因名全称Fibroblast growth factor receptor 2
推荐稀释比
Western blot (WB) 1:500~2000
Immunocoprecipitation 1:20

相关搜索:FGFR2抗体FGFR2单抗Anti-FGFR2 Antibody
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