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Lipoprotein Lipase 抗体

LPL 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2C5 unconjugated
产品编号 ABIN969262
发货至: 中国
  • 抗原 See all Lipoprotein Lipase (LPL) 抗体
    Lipoprotein Lipase (LPL)
    适用
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    宿主
    • 65
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    小鼠
    克隆类型
    • 61
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    单克隆
    标记
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    This Lipoprotein Lipase antibody is un-conjugated
    应用范围
    • 66
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    Western Blotting (WB), ELISA
    原理
    LPL Antibody
    纯化方法
    Ascitic fluid
    免疫原
    Purified recombinant fragment of LPL expressed in E. Coli.
    克隆位点
    2C5
    亚型
    IgG1
    Top Product
    Discover our top product LPL Primary Antibody
  • 应用备注
    ELISA: 1/10000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Ascitic fluid containing 0.03 % sodium azide.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Chen, Jou, Fann, Chen, Chung, Lin, Wu, Kang, Chen, Jong, Lo, Kang, Chen, Chang, Huang, Wu, Pan: "Lipoprotein lipase variants associated with an endophenotype of hypertension: hypertension combined with elevated triglycerides." in: Human mutation, Vol. 30, Issue 1, pp. 49-55, (2009) (PubMed).

    Berk, Johnson, Lee, Zhang, Boozer, Pi-Sunyer, Fried, Albu: "Higher post-absorptive skeletal muscle LPL activity in African American vs. non-Hispanic White pre-menopausal women." in: Obesity (Silver Spring, Md.), Vol. 16, Issue 1, pp. 199-201, (2008) (PubMed).

  • 抗原
    Lipoprotein Lipase (LPL)
    别名
    LPL (LPL 产品)
    别名
    HDLCQ11 antibody, LIPD antibody, fb62e04 antibody, fc49b03 antibody, wu:fb62e04 antibody, wu:fc49b03 antibody, LPL antibody, lipd antibody, hdlcq11 antibody, lpl antibody, LOC100223817 antibody, lipoprotein lipase antibody, LPL antibody, Lpl antibody, lpl antibody
    背景

    Description: LPL: lipoprotein lipase, also known as LIPD, HDLCQ11. Entrez Protein: NP_000228. It is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism.

    Aliases: LIPD, HDLCQ11

    分子量
    53.1kDa
    基因ID
    4023
    HGNC
    4023
    UniProt
    P06858
    途径
    Lipid Metabolism
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