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connexin-30 Antibody Blocking

Peptide(bs-23115P)-500ug
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  • ¥880
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  • bs-23115P
  • 2025年10月16日
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      500ug

    产品编号bs-23115P
    英文名称connexin-30 Antibody Blocking Peptide
    中文名称间隙连接蛋白30/GJB6封闭多肽
    英文别名Connexin 30; Connexin-30; Cx30; CXB6_HUMAN; DFNA3; ectodermal dysplasia 2, hidrotic (Clouston syndrome); ED2; EDH; Gap junction beta 6 protein; Gap junction beta-6 protein; gap junction protein, beta 6 (connexin 30); gap junction protein, beta 6; GJB6; HED; NSRD1.
    纯化方法HPLC
    研究领域

    Neuroscience > Sensory System > Auditory system

    Signal Transduction > Cytoskeleton / ECM > Cell Adhesion > Gap Junctions

    亚基A connexon is composed of a hexamer of connexins. Interacts with CNST
    亚细胞定位Cell membrane; Multi-pass membrane protein. Cell junction, gap junction.
    相似性Belongs to the connexin family. Beta-type (group I) subfamily.
    功能One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neiGHBoring cell.
    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The connexin family of proteins form hexameric complexes called connexons that facilitate movement of low molecular weight proteins between cells via gap junctions. Connexin proteins share a common topology of four transmembrane alpha-helical domains, two extracellular loops, a cytoplasmic loop and cytoplasmic N- and C-termini. Many of the key functional differences between connexins arise from specific amino-acid substitutions in the most highly conserved domains: the transmembrane and extracellular regions. Connexin 30, also known as GJB6 (Gap junction beta 6), ED2, EDH, HED or DFNA3, is a 261 amino acid multi-pass membrane protein that localizes to the cell junction and belongs to the connexin family. Functioning as a hexamer with other connexin proteins, connexin 30 facilitates the diffusion of low molecular weight materials from one cell to another. Defects in the gene encoding connexin 30 are the cause of ectodermal dysplasia type 2 (ED2) and non-syndromatic sensorineural deafness autosomal dominant type 3 (DFNA3), the former of which is characterized by abnormal development of ectodermal structures (such as skin and nails).

     

     

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