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GPD1L Antibody Blocking Peptid

e(bs-16274P)-500ug
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  • bs-16274P
  • 2025年10月16日
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      500ug

    产品编号bs-16274P
    英文名称GPD1L Antibody Blocking Peptide
    中文名称甘油-3-磷酸脱氢酶1样封闭多肽
    英文别名2210409H23Rik; D9Ertd660e; Glycerol 3 phosphate dehydrogenase 1 like; Glycerol 3 phosphate dehydrogenase 1 like protein; Glycerol-3-phosphate dehydrogenase 1-like protein; GPD 1L; GPD1-L; gpd1l; GPD1L_HUMAN; KIAA0089; RGD1560123.
    纯化方法HPLC
    亚细胞定位Cytoplasm. Localized to the region of the plasma membrane.
    组织特异性Most highly expressed in heart tissue, with lower levels in the skeletal muscle, kidney, lung and other organs.
    相似性Belongs to the NAD-dependent glycerol-3-phosphate dehydrogenase family.
    功能Play a role in regulating cardiac sodium current; decreased enzymatic activity with resulting increased levels of glycerol 3-phosphate activating the DPD1L-dependent SCN5A phosphorylation pathway, may ultimately lead to decreased sodium current; cardiac sodium current may also be reduced due to alterations of NAD(H) balance induced by DPD1L.
    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The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). [provided by RefSeq, Jul 2010]

     

     

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