CDH23 Antibody Blocking Peptide(bs-15498P)-500ug

CDH23 Antibody Blocking Peptid

e(bs-15498P)-500ug
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  • bs-15498P
  • 2025年10月16日
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      500ug

    产品编号bs-15498P
    英文名称CDH23 Antibody Blocking Peptide
    中文名称钙粘蛋白23封闭多肽
    英文别名Cadherin like 23; Age related hearing loss 1; Ahl 1; Ahl; Ahl1; Bob; Bobby; Bus; Bustling; Cadherin 23; Cadherin23; Cadherin-23; CDH 23; Mdfw; Modifier of deaf waddler; nmf112; nmf181; nmf252; Otocadherin; USH 1D; USH1 D; USH1D; Waltzer; CAD23_HUMAN.
    纯化方法HPLC
    研究领域

    Neuroscience > Sensory System > Auditory system

    Neuroscience > Sensory System > Visual system

    Signal Transduction > Cytoskeleton / ECM > Cell Adhesion > Cadherins

    亚基Interacts with PCDH15. Interacts with USH1C and USH1G.
    亚细胞定位Cell membrane; Single-pass type I membrane protein.
    组织特异性Particularly strong expression in the retina. Found also in the cochlea.
    相似性Contains 27 cadherin domains.
    功能Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells. CDH23 is required for establishing and/or maintaining the proper organization of the stereocilia bundle of hair cells in the cochlea and the vestibule during late embryonic/early postnatal development. It is part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.
    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This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described. [provided by RefSeq, May 2013].

     

     

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