Cell Signaling Technology

Product Pathways - Tyrosine Kinase / Adaptors

Phospho-FGF Receptor (Tyr653/654) Antibody #3471

fgf   fgfr   fibroblast growth factor receptor  

No. Size Price
3471S 100 µl ( 10 western blots ) ¥4,050.00 现货查询 购买询价 防伪查询
3471 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human, Endogenous 120, 145 Rabbit

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting,


Species predicted to react based on 100% sequence homology: Mouse, Rat,

Specificity / Sensitivity

Phospho-FGF Receptor (Tyr653/654) Antibody detects transfected levels of FGF receptors only when phosphorylated at tyrosines 653/654. This antibody cross-reacts with activated PDGF receptor and insulin/IGF-I receptors.

磷酸化FGF Receptor (Tyr653/654) 抗体仅在Tyr653/654被磷酸化后才能检测到转染表达的FGFR蛋白的存在。本抗体能与活化的PDGF和胰岛素IGF-I receptors交叉反应。

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Tyr653/654 of human FGFR-1 (the corresponding sequence is the same in FGFR-2, -3 and -4). Antibodies are purified by protein A and peptide affinity chromatography.

多克隆抗体通过用多肽免疫动物得到,该多肽是根据人的FGFR-1蛋白Tyr653/654附近的氨基酸序列(与 FGFR-2, -3 and -4上对应的序列相同)合成的。抗体经过protein A和亲和层析纯化。

Western Blotting

Western Blotting

Western blot analysis of extracts from 293 cells overexpressing human FGFR-1, untreated or calf intestinal phosphatase (CIP)-treated, using Phospho-FGF Receptor (Tyr653/654) Antibody (upper) or FGF Receptor 1 Antibody #3472 (lower). Overexpression of human FGFR-1 protein in 293 cells results in constitutive activation of the receptors (courtesy of Dr. Pamela Maher, personal communication). CIP treatment abolishes the reactivity of this antibody to FGFR-1.Western blot法检测高表达人FGFR1的293细胞提取物:经过或未经calf intestinal phosphatase (CIP)处理。使用抗体为:Phospho-FGF Receptor (Tyr653/654) Antibody(上)或FGF Receptor 1 Antibody #3472(下)。293细胞高表达人FGFR-1蛋白后使受体组成型激活(courtesy of Dr. Pamela Maher, personal communication)。CIP 处理则能破坏本抗体对FGFR-1的反应。

Western Blotting

Western Blotting

Western blot analysis of extracts from A-204 cells treated with or without bFGF, using Phospho-FGF Receptor (Tyr653/654) Antibody (upper) and FGF Receptor 1 (D8E4) XP® Rabbit mAb (lower).


Fibroblast growth factors (FGFs) produce mitogenic and angiogenic effects in target cells by signaling through cell surface receptor tyrosine kinases. There are four members of the FGF receptor family: FGFR-1 (flg), FGFR-2 (bek, KGFR), FGFR-3, and FGFR-4. Each receptor contains an extracellular ligand binding domain, a transmembrane domain, and a cytoplasmic kinase domain (1). Following ligand binding and dimerization, the receptors are phosphorylated at specific tyrosine residues (2). Seven tyrosine residues in the cytoplasmic tail of FGFR-1 can be phosphorylated: Tyr463, 583, 585, 653, 654, 730, and 766. Tyr653 and Tyr654 are important for catalytic activity of activated FGFR and are essential for signaling (3). The other phosphorylated tyrosine residues may provide docking sites for downstream signaling components such as Crk and PLCγ (4,5).

成纤维细胞生长因子 (FGFs)通过细胞表面的酪氨酸激酶受体传递信号,对靶细胞产生促有丝分裂和血管生成的效应。已知FGF受体家族有四个成员:FGFR-1 (flg), FGFR-2 (bek, KGFR), FGFR-3和FGFR-4。每个受体都有一个胞外配体结合区、跨膜区和一个胞内激酶区(1)。在结合配体和二聚化之后,受体的特定的酪氨酸位点发生磷酸化(2)。在FGFR-1的羧基端有7个酪氨酸位点能被磷酸化:Tyr463, 583, 585, 653, 654, 730和 766。Tyr653 和Tyr654对激活的FGFR的催化活性十分重要,对信号传导也是必要的(3)。其它的磷酸化酪氨酸位点能够为下游信号分子,如Crk 和PLCγ,提供结合位点(4,5)。

  1. Powers, C.J. et al. (2000) Endocr Relat Cancer 7, 165-97.
  2. Reilly, J.F. et al. (2000) J Biol Chem 275, 7771-8.
  3. Mohammadi, M. et al. (1996) Mol Cell Biol 16, 977-89.
  4. Mohammadi, M. et al. (1991) Mol Cell Biol 11, 5068-78.
  5. Larsson, H. et al. (1999) J Biol Chem 274, 25726-34.

Application References

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