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PGAM2 抗体 (AA 1-253)

This anti-PGAM2 antibody is a 小鼠 单克隆 antibody detecting PGAM2 in WB, IF, ELISA 和 ICC. Suitable for 人.
产品编号 ABIN5776232
发货至: 中国

Quick Overview for PGAM2 抗体 (AA 1-253) (ABIN5776232)

抗原

See all PGAM2 抗体
PGAM2 (phosphoglycerate Mutase 2 (Muscle) (PGAM2))

适用

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宿主

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小鼠

克隆类型

  • 29
  • 5
单克隆

标记

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This PGAM2 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunofluorescence (IF), ELISA, Immunocytochemistry (ICC)

克隆位点

AT5A7
  • 抗原表位

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    AA 1-253

    免疫原

    Recombinant human PGAM2 (1-253aa) purified from E. coli

    亚型

    IgG2b kappa
  • 限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    储存条件

    4 °C,-20 °C,-80 °C

    储存方法

    Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
  • 抗原

    PGAM2 (phosphoglycerate Mutase 2 (Muscle) (PGAM2))

    别名

    PGAM2

    背景

    Phosphoglycerate mutase (PGAM) catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. Since both 3-PGA and 2-PGA are allosteric regulators of the pentose phosphate pathway (PPP) and glycine and serine synthesis pathways, respectively, PGAM2 may contribute to the biosynthesis of amino acids, 5-carbon sugar, and nucleotides precursors. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). Mutations in this gene cause muscle phosphoglycerate mutase deficiency, also known as glycogen storage disease X. PGAM2 is one of two PGAM subunits found in humans and is predominantly expressed in adult muscle.

    NCBI登录号

    NP_000281
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