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MOCS1 抗体 (AA 52-584)

The 兔 多克隆 anti-MOCS1 antibody (ABIN7875568) specifically detects MOCS1 in WB, ELISA 和 IF. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7875568
发货至: 中国
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Quick Overview for MOCS1 抗体 (AA 52-584) (ABIN7875568)

抗原

See all MOCS1 抗体
MOCS1 (Molybdenum Cofactor Synthesis 1 (MOCS1))

适用

  • 30
  • 18
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 32

克隆类型

  • 32
多克隆

标记

  • 22
  • 2
  • 2
  • 2
  • 2
  • 2
This MOCS1 antibody is un-conjugated

应用范围

  • 32
  • 19
  • 14
  • 6
  • 4
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF)
  • 抗原表位

    • 8
    • 8
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 52-584

    原理

    MOCS1 Antibody

    纯化方法

    Antigen affinity chromatography

    免疫原

    An E.coli-derived human recombinant protein (amino acids E52-R584) was used as the immunogen for the MOCS1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the MOCS1 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the MOCS1 Antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    MOCS1 (Molybdenum Cofactor Synthesis 1 (MOCS1))

    别名

    MOCS1

    背景

    Molybdenum cofactor biosynthesis protein 1 is a protein that in humans and other animals, fungi, and cellular slime molds, is encoded by the MOCS1 gene. Molybdenum cofactor biosynthesis is a conserved pathway leading to the biological activation of molybdenum. The protein encoded by this gene is involved in this pathway. This gene was originally thought to produce a bicistronic mRNA with the potential to produce two proteins (MOCS1A and MOCS1B) from adjacent open reading frames. However, only the first open reading frame (MOCS1A) has been found to encode a protein from the putative bicistronic mRNA, whereas additional splice variants are likely to produce a fusion between the two open reading frames. This gene is defective in patients with molybdenum cofactor deficiency, type A. A related pseudogene has been identified on chromosome 16.

    UniProt

    Q9NZB8
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