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Lipoprotein Lipase 抗体

LPL 适用: 人 WB, ICC, IF, IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2854941
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
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    克隆类型
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    多克隆
    标记
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    This Lipoprotein Lipase antibody is un-conjugated
    应用范围
    • 62
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    Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    小鸡, 人, 小鼠, 绵羊
    产品特性
    Rabbit Polyclonal antibody to LPL (lipoprotein lipase)
    LPL antibody
    纯化方法
    Purified by antigen-affinity chromatography.
    免疫原
    Recombinant protein encompassing a sequence within the center region of human LPL. The exact sequence is proprietary.
    亚型
    IgG
    Top Product
    Discover our top product LPL Primary Antibody
  • 应用备注
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.11 mg/mL
    缓冲液
    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.025 % ProClin 300
    储存液
    ProClin
    注意事项
    This product contains ProClin: 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 as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原
    Lipoprotein Lipase (LPL)
    别名
    lipoprotein lipase (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
    LPL encodes lipoprotein lipase, which 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.

    Cellular Localization: Cell membrane, Lipid-anchor , GPI-anchor , Secreted
    分子量
    53 kDa
    基因ID
    4023
    UniProt
    P06858
    途径
    Lipid Metabolism
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