Utrophin Antibody Blocking Peptide(bs-11394P)-500ug

Utrophin Antibody Blocking Pep

tide(bs-11394P)-500ug
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  • ¥880
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  • bs-11394P
  • 2025年10月16日
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      500ug

    产品编号bs-11394P
    英文名称Utrophin Antibody Blocking Peptide
    中文名称肌营养不良蛋白相关蛋白1封闭多肽
    英文别名DMDL; DRP 1; DRP; DRP-1; DRP1; Dystrophin like protein; Dystrophin related protein 1; Dystrophin related protein; Dystrophin-related protein 1; FLJ23678; UTRN; UTRO_HUMAN; Utrophin (homologous to dystrophin); Utrophin
    纯化方法HPLC
    研究领域

    Neuroscience > Cell Type Marker > Neuron marker > Synapse marker

    Signal Transduction > Cytoskeleton / ECM > Cytoskeleton > Microfilaments > Actin etc > Actin Binding Proteins

    亚基Interacts with the syntrophins SNTA1; SNTB1 and SNTB2. Interacts with SYNM. Interacts (via its WWW and ZZ domains) with DAG1 (via the PPXY motif of betaDAG1); the interaction is inhibited by the tyrosine phosphorylation of the PPXY motif of DAG1.
    亚细胞定位Cell junction > synapse > postsynaptic cell membrane. Cytoplasm > cytoskeleton. Neuromuscular junction.
    组织特异性Muscle.
    相似性Contains 2 CH (calponin-homology) domains.
    Contains 20 spectrin repeats.
    Contains 1 WW domain.
    Contains 1 ZZ-type zinc finger.
    功能May play a role in anchoring the cytoskeleton to the plasma membrane.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料Dystrophin and utrophin are related structural, Actin-binding proteins that are involved in anchoring the cytoskeleton to the plasma membrane. Dystrophin is the protein product of the Duchenne/Becker muscular dystrophy gene. Dystrophin expression is found in muscle and brain tissues, where it is localized to the inner surface of the plasma membrane. It has been speculated that alternative splicing of the carboxy terminus allows dystrophin to interact with a variety of proteins. Research has shown that the loss of dystrophin-associated proteins in Duchenne afflicted muscle is due to the absence of dystrophin rather than to muscle degradation and that the lack of dystrophin results in the loss of linkage between the cytoskeleton and the extracellular matrix. Evidence suggests that the upregulation of utrophin can reduce the dystrophic pathology.

     

     

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