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MVK 抗体

This anti-MVK antibody is a 兔 多克隆 antibody detecting MVK in WB. Suitable for 人.
产品编号 ABIN2854359
发货至: 中国

Quick Overview for MVK 抗体 (ABIN2854359)

抗原

See all MVK 抗体
MVK (Mevalonate Kinase (MVK))

适用

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宿主

  • 40
  • 5

克隆类型

  • 41
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多克隆

标记

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This MVK antibody is un-conjugated

应用范围

  • 33
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Western Blotting (WB)
  • 交叉反应

    产品特性

    Rabbit Polyclonal antibody to MVK (mevalonate kinase)
    MVK antibody [N1C2]

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human MVK. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: 293T

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): 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

    MVK (Mevalonate Kinase (MVK))

    别名

    mevalonate kinase

    背景

    This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash. Two transcript variants that encode the same protein have been found for this gene.

    Cellular Localization: Cytoplasm , Peroxisome

    分子量

    42 kDa

    基因ID

    4598

    UniProt

    Q03426
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