人成纤维细胞生长因子受体2检测试剂盒,BR

产品属性 Product Attributes

基本信息

中文名称： 人成纤维细胞生长因子受体2检测试剂盒
英文名称： Human FGFR2 ELISA Kit
别名： Fibroblast Growth Factor Receptor 2; BBDS; BEK; BFR-1; CD332; CEK3; CFD1; craniofacial dysostosis 1; ECT1; FGFR2; Jackson-Weiss syndrome; JWS; Keratinocyte growth factor receptor like 14; KGFR; KSAM; soluble FGFR4 variant 4; TK14
储存条件： 2-8℃，6 months
规格： 48T ; 96T
检测目标： FGFR2/CD332
样品类型： 血清/血浆/细胞培养上清
反应性： Human
应用： ELISA
定量/定性： 定量检测
检测范围： 43.75-2800pg/mL
灵敏度： 22pg/mL
精密度： 板内，板间变异系数均<10%
回收率： 80%-120%

Elisa信息

Swiss Prot： P21802
Gene ID： 2263
背景说明： FGFR2, also known as CD332, belongs to the fibroblast growth factor receptor subfamily where amino acid sequence is highly conserved between members and throughout evolution. FGFR2 acts as cell-surface receptor for fibroblast growth factors and plays an essential role in the regulation of cell proliferation, differentiation, migration and apoptosis, and in the regulation of embryonic development. It is required for normal embryonic patterning, trophoblast function, limb bud development, lung morphogenesis, osteogenesis and skin development. FGFR2 plays an essential role in the regulation of osteoblast differentiation, proliferation and apoptosis, and is required for normal skeleton development. It also promotes cell proliferation in keratinocytes and imature osteoblasts, but promotes apoptosis in differentiated osteoblasts. FGFR2 signaling is down-regulated by ubiquitination, internalization and degradation. Mutations that lead to constitutive kinase activation or impair normal CD332 maturation, internalization and degradation lead to aberrant signaling. Over-expressed FGFR2 promotes activation of STAT1. Defects in CD3322 are the cause of Crouzon syndrome, Jackson-Weiss syndrome, Apert syndrome, Pfeiffer syndrome, Beare-Stevenson cutis gyrata syndrome, familial scaphocephaly syndrome, lacrimo-auriculo-dento-digital syndrome and Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis.

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注意事项 Considerations

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