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Phospho-Ezrin (Thr567)/Radixin

(Thr564)/Moesin (Thr558) Antibody
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月26日
  • W
  • Rabbit
  • H,M,R,Mk,X
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-Ezrin (Thr567)/Radixin (Thr564)/Moesin (Thr558) Antibody

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Thr567 of human ezrin

    • 应用范围

      W

    • 宿主

      Rabbit

    • 适应物种

      H,M,R,Mk,X

    • 保质期

      详见说明书

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 是否单克隆

      2

    • 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  Mk=Monkey  X=Xenopus
    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 R Mk (X) Endogenous 75 Moesin. 80 Ezrin, Radixin. Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-Ezrin (Thr567)/Radixin (Thr564)/Moesin (Thr558) Antibody detects endogenous levels of ezrin, radixin and moesin only when phosphorylated at threonine 567, 564 or 558, respectively. This antibody does not cross-react with related phospho-proteins such as merlin or band 4.1.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Thr567 of human ezrin. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from A431 cells, untreated or EGF-treated, using Phospho-Ezrin (Thr567)/Radixin (Thr564)/Moesin (Thr558) Antibody (left) or Ezrin/Radixin/Moesin Antibody #3142 (right).

    Background

    The ezrin, radixin, and moesin (ERM) proteins function as linkers between the plasma membrane and the actin cytoskeleton and are involved in cell adhesion, membrane ruffling, and microvilli formation (1). ERM proteins undergo intra or intermolecular interaction between their amino- and carboxy-terminal domains, existing as inactive cytosolic monomers or dimers (2). Phosphorylation at a carboxy-terminal threonine residue (Thr567 of ezrin, Thr564 of radixin, Thr558 of moesin) disrupts the amino- and carboxy-terminal association and may play a key role in regulating ERM protein conformation and function (3,4). Phosphorylation at Thr567 of ezrin is required for cytoskeletal rearrangements and oncogene-induced transformation (5). Ezrin is also phosphorylated at tyrosine residues upon growth factor stimulation. Phosphorylation of Tyr353 of ezrin transmits a survival signal during epithelial differentiation (6).

    1. Tsukita, S. and Yonemura, S. (1999) J. Biol. Chem. 274, 34507-34510.
    2. Mangeat, P. et al. (1999) Trends Cell Biol. 9, 187-192.
    3. Matsui, T. et al. (1998) J. Cell Biol. 140, 647-657.
    4. Gautreau, A. et al. (2000) J. Cell Biol. 150, 193-203.
    5. Tran Quang, C. et al. (2000) EMBO J. 19, 4565-4576.
    6. Gautreau, A. et al. (1999) Proc. Natl. Acad. Sci. USA 96, 7300-7305.
    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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    图标文献和实验
    相关实验
    • Using Phospho‐Motif Antibodies to Determine Kinase Substrates

      comprising both the phosphorylated residue and the surrounding residues that determine kinase specificity, with degenerate residues taking up the remaining positions. Currently, several categories of phospho?motif antibody are commercially available

    • 运用Cell Based Elisa检测信号通路蛋白和磷酸化蛋白

      using Phospho-p38 antibody (A) and Total-p38 antibody (B). Cell Based Elisa were performed directly in the 96-well plates using Phospho-p38 and Total-p38 antibodies (C). Figure 3: JNK detection with FACECells were serum-starved for 16 hours

    • 【求助】PKC激活程度测定

      9921 Phospho-PKC Antibody Sampler Kit 9375 Phospho-PKCalpha/beta II (Thr638/641) Antibody W IP 9374 Phospho-PKCdelta (Thr505) Antibody W IHC 9376 Phospho-PKCdelta/theta (Ser643/676) Antibody W IHC 9377 Phospho-PKCtheta (Thr538

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