CHM Antibody Blocking Peptide(bs-13911P)-500ug

CHM Antibody Blocking Peptide(

bs-13911P)-500ug
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  • bs-13911P
  • 2025年10月16日
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      500ug

    产品编号bs-13911P
    英文名称CHM Antibody Blocking Peptide
    中文名称遗传性脉络膜缺乏症相关蛋白封闭多肽
    英文别名CHM; Chm; Choroideraemia protein; Choroideremia; DXS540; FLJ38564; GGTA; HSD 32; MGC102710; Rab escort protein 1; Rab geranylgeranyltransferase component A; Rab proteins geranylgeranyltransferase component A 1; RAE1_HUMAN; REP 1; REP-1; REP1; TCD; TCD protein.
    纯化方法HPLC
    研究领域

    Neuroscience > Neurotransmission > Secretory Vesicles > Rabs

    Signal Transduction > Protein Trafficking > Chaperones > Other Chaperones

    Signal Transduction > Protein Trafficking > Vesicle Transport > Regulation

    亚细胞定位Belongs to the Rab GDI family.
    功能Binds unprenylated Rab proteins, presents it to the catalytic Rab GGTase dimer, and remains bound to it after the geranylgeranyl transfer reaction. The component A is thought to be regenerated by transferring its prenylated Rab back to the donor membrane. Also a pre-formed complex consisting of CHM and the Rab GGTase dimer (RGGT or component B) can bind to and prenylate Rab proteins; this alternative pathway is proposed to be the predominant pathway for Rab protein geranylgeranylation.
    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 encodes component A of the RAB geranylgeranyl transferase holoenzyme. In the dimeric holoenzyme, this subunit binds unprenylated Rab GTPases and then presents them to the catalytic Rab GGTase subunit for the geranylgeranyl transfer reaction. Rab GTPases need to be geranylgeranyled on either one or two cysteine residues in their C-terminus to localize to the correct intracellular membrane. Mutations in this gene are a cause of choroideremia; also known as tapetochoroidal dystrophy (TCD). This X-linked disease is characterized by progressive dystrophy of the choroid, retinal pigment epithelium and retina. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Feb 2009]

     

     

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