产品封面图

Phospho-IGF-I Receptor β (Tyr1

135/1136)/Insulin Receptor β (Tyr1150/1151) (19H7) Rabbit mAb
收藏
  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月19日
  • W
  • H,M,R,B
avatar
品牌商
13钻石会员
  • 企业认证

    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-IGF-I Receptor β (Tyr1135/1136)/Insulin Receptor β (Tyr1150/1151) (19H7) Rabbit mAb

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Tyr1135/1136 of human IGF-I receptor β

    • 应用范围

      W

    • 库存

      大量

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 适应物种

      H,M,R,B

    • 供应商

      CST

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/300 ul (30 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:300 ul (30 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  R=Rat  B=Bovine
    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) Isotype
    W H M R (B) Endogenous 95 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    Phospho-IGF-I Receptor β (Tyr1135/1136)/Insulin Receptor β (Tyr1150/1151) (19H7) Rabbit mAb detects endogenous levels of IGF-I receptor and insulin receptor only when phosphorylated at tyrosine 1135/1136 or tyrosine 1150/1151, respectively. It does not cross-react with other related tyrosine-phosphorylated tyrosine kinases.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Tyr1135/1136 of human IGF-I receptor β.

    Western Blotting

    Western Blotting

    Western blot analysis of untreated and IGF-treated Hela cell extracts as well as untreated and insulin-treated H-4-II-E cell extracts using Phospho-IGF-I-Receptor beta (Tyr1135/1136)/Insulin Receptor beta (Tyr1150/1151)(19H7) Rabbit mAb

    Western Blotting

    Western Blotting

    Phospho-IGF-I Receptorβ (Tyr1135/1136)/Insulin Receptor β (Tyr1150/1151) (19H7) Rabbit mAb specifically binds to tyrosine phosphorylated IGF-1 and insulin receptors, but not other phosphorylated tyrosine kinases. Western blot analysis of of extracts from cells expressing different activated tyrosine kinase proteins, using Phospho-IGF-I Receptor β (Tyr1135/1136)/Insulin Receptor β(Tyr1150/1151) (19H7) Rabbit mAb (upper) or Phospho-Tyrosine Mouse mAb (P-Tyr-100) #9411 (lower).

    Background

    Type I insulin-like growth factor receptor (IGF-IR) is a transmembrane receptor tyrosine kinase that is widely expressed in many cell lines and cell types within fetal and postnatal tissues (1-3). Receptor autophosphorylation follows binding of the IGF-I and IGF-II ligands. Three tyrosine residues within the kinase domain (Tyr1131, Tyr1135, and Tyr1136) are the earliest major autophosphorylation sites (4). Phosphorylation of these three tyrosine residues is necessary for kinase activation (5,6). Insulin receptors (IRs) share significant structural and functional similarity with IGF-I receptors, including the presence of an equivalent tyrosine cluster (Tyr1146/1150/1151) within the kinase domain activation loop. Tyrosine autophosphorylation of IRs is one of the earliest cellular responses to insulin stimulation (7). Autophosphorylation begins with phosphorylation at Tyr1146 and either Tyr1150 or Tyr1151, while full kinase activation requires triple tyrosine phosphorylation (8).

    1. Adams, T.E. et al. (2000) Cell. Mol. Life Sci. 57, 1050-1093.
    2. Baserga, R. et al. (2000) Oncogene 19, 5574-5581.
    3. Scheidegger, K.J. et al. (2000) J. Biol. Chem. 275, 38921-38928.
    4. Hernandez-Sanchez, C. et al. (1995) J. Biol. Chem. 270, 29176-29181.
    5. Lopaczynski, W. et al. (2000) Biochem. Biophys. Res. Commun. 279, 955-960.
    6. Baserga, R. et al. (1999) Exp. Cell Res. 253, 1-6.
    7. White, M.F. et al. (1985) J. Biol. Chem. 260, 9470-9478.
    8. White, M.F. et al. (1988) J. Biol. Chem. 263, 2969-2980.
    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

    Rabbit Monoclonals Produced Using Epitomics® Technology, U.S. Patent No. 5,675,063.


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

    风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。

    图标文献和实验
    相关实验
    • 乙-受体(β-受体) β-receptor

      乙 -受体(β -受体) β -receptor 儿茶酚胺的受体之一。一般呈抑制反应,即一旦接受儿茶酚胺的作用,便产生血管、子宫、支气管等器管的舒张和心肌兴奋。由异丙基肾上腺素( isopr-oterenol)的作用也可产生这种反应。而 3, 4-二氯异丙基肾上腺素( DCI)、心得安等β -受体阻断剂可阻断其作用。  

    • β受体 β-receptor

         为儿茶酚胺受体之一。一般为抑制的反应,儿茶酚胺与β受体作用可引起血管、子宫和支气管肌等弛缓和心脏兴奋。异丙基肾上腺素也可使之产生效应。3,4-二氯异丙基肾上腺素(DCI)和萘异丙仲胺等β巡断剂可阻抑其作用。  

    • Electrophoretic Mobility Shift Assay for Detection of DNA Binding Proteins Recognizing β-Adrenergic Receptor Gene Sequences

      The β-adrenergic receptors (β-ARs) are important modulators in the sympathetic control of various metabolic processes in the central (CNS) and peripheral nervous system (1 –4 ). The β-ARs mediate the physiological effects of the catecholamines

    图标技术资料

    暂无技术资料 索取技术资料

    同类产品报价

    产品名称
    产品价格
    公司名称
    报价日期
    Phospho-IGF-I Receptor β (Tyr1135/1136)/Insulin Receptor β (Tyr1150/1151) (19H7) Rabbit mAb
    询价