ESYT1 Antibody Blocking Peptide(bs-11002P)-500ug

ESYT1 Antibody Blocking Peptid

e(bs-11002P)-500ug
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  • bs-11002P
  • 2025年10月16日
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      500ug

    产品编号bs-11002P
    英文名称ESYT1 Antibody Blocking Peptide
    中文名称延伸突触蛋白1封闭多肽
    英文别名Extended synaptotagmin 1; KIAA0747; E Syt1; E-Syt1; Esyt1; ESYT1_HUMAN; Extended synaptotagmin like protein 1; Extended synaptotagmin-1; Family with sequence similarity 62 (C2 domain containing) member A; Family with sequence similarity 62 member A; MBC2; Membrane bound C2 domain containing protein; Membrane-bound C2 domain-containing protein; Protein FAM62A.
    纯化方法HPLC
    研究领域

    Cell Biology > Other Antibodies > Other Antibodies

    亚细胞定位Membrane. Localizes to intracellular membranes.
    组织特异性Widely expressed.
    相似性Belongs to the extended synaptotagmin family.
    Contains 5 C2 domains.
    功能May play a role as calcium-regulated intrinsic membrane protein.
    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Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.

     

     

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