FGF Receptor 3 Antibody

FGF Receptor 3 Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年07月13日
  • W
  • Rabbit
  • H,M
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    • 详细信息
    • 技术资料
    • 抗体英文名

      FGF Receptor 3 Antibody

    • 抗原

      synthetic peptide corresponding to the sequence surrounding His111 of human FGF receptor 3

    • 应用范围

      W

    • 宿主

      Rabbit

    • 供应商

      CST

    • 保质期

      详见说明书

    • 适应物种

      H,M

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting
    Reactivity Key:  H=Human  M=Mouse
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W H M Endogenous 145 Rabbit
    Protocols
    Specificity / Sensitivity

    FGF Receptor 3 Antibody detects endogenous levels of total FGF receptor 3 protein. This antibody does not cross-react with other FGF receptor family members.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence surrounding His111 of human FGF receptor 3. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Kms-11 cell lysates using FGF Receptor 3 Antibody.

    Background

    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: FGFR1 (flg), FGFR2 (bek, KGFR), FGFR3, and FGFR4. 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 FGFR1 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).

    FGFR-3 participates in a diverse array of biological processes, including cell growth, differentiation, and migration. Activating mutations in FGFR-3 are associated with multiple myeloma, cervical carcinoma, and bladder cancer and it represents a potential target for therapy (6).

    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.
    6. Knowles, M.A. (2008) Future Oncol 4, 71-83.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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