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GLYATL1 Antibody Blocking Pept

ide(bs-13444P)-500ug
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  • ¥880
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  • bs-13444P
  • 2025年10月16日
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      500ug

    产品编号bs-13444P
    英文名称GLYATL1 Antibody Blocking Peptide
    中文名称甘胺酸-N-酰基转移酶样1封闭多肽
    英文别名Acyl CoA glycine N acyltransferase like protein 1; EC 2.3.1.13; FLJ26507; FLJ34646; GATF C; GATFC; Glycine N acyltransferase like 1; GNAT; MGC15397; MGC15937; GLYL1_HUMAN.
    纯化方法HPLC
    研究领域

    Metabolism > Pathways and Processes > Metabolic signaling pathways > Amino acid metabolism

    Metabolism > Pathways and Processes > Mitochondrial Metabolism > Mitochondrial markers

    Signal Transduction > Metabolism > Amino Acids

    Signal Transduction > Metabolism > Mitochondrial

    亚细胞定位Mitochondrial
    组织特异性Expressed in liver and kidney and, at lower levels, in pancreas, testis, ovary and stomach.
    相似性Belongs to the glycine N-acyltransferase family.
    功能GLYATL1 is a mitochondrial acyltransferase which transfers the acyl group to the N-terminus of glycine. It can conjugate a multitude of substrates to form a variety of N-acylglycines.
    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GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

     

     

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