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HSP22 Antibody Blocking Peptid

e(bs-3672P)-500ug
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  • bs-3672P
  • 2025年10月16日
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      500ug

    产品编号bs-3672P
    英文名称HSP22 Antibody Blocking Peptide
    中文名称热休克蛋白-22封闭多肽
    英文别名CMT2L; CRYAC; DHMN 2; DHMN2; E2 induced gene 1 protein; E2IG1; H11; Heat shock 22kDa protein 8; Heat shock protein 22; Heat shock protein beta 8; Hereditary motor neuropathy distal; HMN 2; HMN2; HSB8; HSPB 8; HSPB8; Protein kinase H11; Small stress protein like protein HSP22; Spinal muscular atrophy distal adult autosomal dominant; Alpha crystallin C chain; Charcot Marie Tooth disease axonal type 2L; Charcot Marie Tooth disease spinal.
    纯化方法HPLC
    研究领域

    Neuroscience > Neurology process > Neurodegenerative disease

    Signal Transduction > Protein Trafficking > Chaperones > Heat Shock Proteins

    亚基Monomer. Interacts with HSPB1. Interacts with DNAJB6.
    亚细胞定位 Cytoplasm. Nucleus. Note=Translocates to nuclear foci during heat shock.
    组织特异性Predominantly expressed in skeletal muscle and heart.
    相似性Belongs to the small heat shock protein (HSP20) family.
    功能Displays temperature-dependent chaperone activity.
    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Hsp22 (HSPB8) is a 196-amino acid protein that contains a central portion homologous to a highly conserved HSP-alpha crystallin domain common to all the small heat shock protein (HSP20) family members. Hsp22 is a monomeric protein which interacts with HSPB1. It displays temperature-dependent chaperone activity. The highest abundance of Hsp22 is in skeletal muscle, heart, and placenta. Mutations in the HSPB8 gene are associated with the inherited peripheral neuropathies, autosomal dominant distal hereditary motor neuropathy type IIA (dSMA) and axonal Charcot-Marie-Tooth disease type 2L (CMT2L).

     

     

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