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Lipoprotein Lipase 抗体

This anti-Lipoprotein Lipase antibody is a 兔 多克隆 antibody detecting Lipoprotein Lipase in WB, ICC, IF 和 IHC (p). Suitable for 人.
产品编号 ABIN2854941
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Lipoprotein Lipase 抗体 (ABIN2854941)

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

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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
  • 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

    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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