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MVK 抗体

MVK 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2854359
发货至: 中国
  • 抗原 See all MVK 抗体
    MVK (Mevalonate Kinase (MVK))
    适用
    • 43
    • 8
    • 7
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 38
    • 5
    克隆类型
    • 40
    • 3
    多克隆
    标记
    • 27
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MVK antibody is un-conjugated
    应用范围
    • 31
    • 16
    • 11
    • 11
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    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
    Top Product
    Discover our top product MVK Primary Antibody
  • 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 (MVK 产品)
    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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