ZSWIM3 Antibody Blocking Peptide(bs-9138P)-500ug

ZSWIM3 Antibody Blocking Pepti

de(bs-9138P)-500ug
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  • bs-9138P
  • 2025年10月16日
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      500ug

    产品编号bs-9138P
    英文名称ZSWIM3 Antibody Blocking Peptide
    中文名称ZSWIM3蛋白封闭多肽
    英文别名Zinc finger SWIM domain containing protein 3; C20orf164; Zinc finger SWIM type containing 3; ZSWIM 3; ZSWM3_HUMAN.
    纯化方法HPLC
    亚基Part of BBSome complex, that contains BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex binds to PCM1 and tubulin. Binds to phosphoinositides.
    亚细胞定位Cell projection, cilium membrane. Cytoplasm. Cytoplasm, cytoskeleton, cilium basal body.
    相似性Belongs to the BBS5 family.
    功能The BBSome complex is required for ciliogenesis but is dispensable for centriolar satellite function. This ciliogenic function is mediated in part by the Rab8 GDP/GTP exchange factor, which localizes to the basal body and contacts the BBSome. Rab8(GTP) enters the primary cilium and promotes extension of the ciliary membrane. Firstly the BBSome associates with the ciliary membrane and binds to RAB3IP/Rabin8, the guanosyl exchange factor (GEF) for Rab8 and then the Rab8-GTP localizes to the cilium and promotes docking and fusion of carrier vesicles to the base of the ciliary 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Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZSWIM3 (Zinc finger SWIM domain-containing protein 3) is a 696 amino acid protein that contains one SWIM-type zinc finger. SWIM domains are found in a variety of eukaryotic and prokaryotic proteins and are thought to be critical for certain ubiquitination reactions. The gene encoding ZSWIM3 maps to human chromosome 20, which contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.

     

     

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