GDE1 | MIR16 Ab Blocking Peptide(bs-12039P)-500ug产品图

GDE1 | MIR16 Ab Blocking Pepti

de(bs-12039P)-500ug
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  • bs-12039P
  • 2026年10月10日
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    • 规格:

      500ug

    产品编号bs-12039P
    英文名称GDE1 Antibody Blocking Peptide
    中文名称膜蛋白相互作用蛋白GDE1 (MIR16) 封闭多肽
    英文别名GDE1; GDE1_HUMAN; EC 3.1.4.44; Glycerophosphodiester phosphodiesterase 1; Glycerophosphoinositol glycerophosphodiesterase GDE1; Membrane interacting protein of RGS16; Membrane-interacting protein of RGS16; RGS16 interacting membrane protein; RGS16-interacting membrane protein; Lysophospholipase D GDE1.
    纯化方法HPLC
    亚基Interacts with RGS16. Interacts with PRAF2.
    亚细胞定位Cytoplasmic. Membrane; Multi-pass membrane protein.
    组织特异性Widely expressed.
    翻译后修饰N-glycosylated
    相似性Belongs to the glycerophosphoryl diester phosphodiesterase family.
    Contains 1 GDPD domain._x000D_
    功能MIR6 has glycerophosphoinositol phosphodiesterase 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GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

     

     

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