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SLC27A5 Antibody

  • 货号:
    CSB-PA876368
  • 规格:
    ¥2024
  • 图片:
    • Western blot analysis of extracts from HepG2 cells, using SLC27A5 antibody.
    • Immunohistochemistry analysis of paraffin-embedded human liver carcinoma tissue using SLC27A5 antibody.
    • Immunofluorescence analysis of A549 cells, using SLC27A5 antibody.
  • 其他:

产品详情

  • 产品名称:
    Rabbit anti-Homo sapiens (Human) SLC27A5 Polyclonal antibody
  • Uniprot No.:
    Q9Y2P5
  • 基因名:
  • 宿主:
    Rabbit
  • 反应种属:
    Human
  • 免疫原:
    Synthesized peptide derived from internal of Human SLC27A5.
  • 免疫原种属:
    Homo sapiens (Human)
  • 克隆类型:
    Polyclonal
  • 纯化方式:
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度:
    It differs from different batches. Please contact us to confirm it.
  • 产品提供形式:
    Liquid
  • 应用范围:
    ELISA,WB,IHC,IF
  • 推荐稀释比:
    Application Recommended Dilution
    WB 1:500-1:3000
    IHC 1:50-1:100
    IF 1:100-1:500
  • Protocols:
  • 储存条件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期:
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

产品评价

靶点详情

  • 功能:
    Acyl-CoA synthetase that catalyzes the activation of bile acids via formation of bile acid CoA thioesters which is necessary for their subsequent conjugation with glycine or taurine. Both primary bile acids (cholic acid and chenodeoxycholic acid) and secondary bile acids (deoxycholic acid and lithocholic acid) are the principal substrates. Also exhibits acyl CoA synthetase activity that activates very long-chain fatty acids (VLCFAs) by catalyzing the formation of fatty acyl-CoA. In vitro, also activates 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanate (THCA), the C27 precursor of cholic acid deriving from the de novo synthesis from cholesterol. Exhibits long-chain fatty acids (LCFA) transport activity. Plays an important role in hepatic fatty acid uptake and bile acid reconjugation and recycling but not in de novo synthesis of bile acids.
  • 基因功能参考文献:
    1. Based on a study of 10 pediatric patients, genetic defects that disrupt bile acid amidation cause fat-soluble vitamin deficiency and growth failure, indicating the importance of bile acid conjugation in lipid absorption. PMID: 23415802
    2. Bile acid-CoA ligase deficiency is a new inborn error of bile acid metabolism [case report] PMID: 22089923
    3. A promoter polymorphism in the FATP5 is associated with the metabolic syndrome and steatosis. PMID: 20945272
  • 亚细胞定位:
    Endoplasmic reticulum membrane; Multi-pass membrane protein. Microsome. Cell membrane; Multi-pass membrane protein.
  • 蛋白家族:
    ATP-dependent AMP-binding enzyme family
  • 组织特异性:
    Predominantly expressed in liver.
  • 数据库链接:

    HGNC: 10999

    OMIM: 603314

    KEGG: hsa:10998

    STRING: 9606.ENSP00000263093

    UniGene: Hs.292177