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GLDC 抗体 (AA 574-1020)

This 兔 多克隆 antibody specifically detects GLDC in WB, ELISA, IHC (p) 和 FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN7875824
发货至: 中国
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Quick Overview for GLDC 抗体 (AA 574-1020) (ABIN7875824)

抗原

See all GLDC 抗体
GLDC (Glycine Dehydrogenase (GLDC))

适用

人, 小鼠, 大鼠

宿主

  • 46
  • 2

克隆类型

  • 46
  • 2
多克隆

标记

  • 22
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GLDC antibody is un-conjugated

应用范围

  • 44
  • 15
  • 13
  • 13
  • 13
  • 9
  • 7
  • 6
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • 抗原表位

    • 15
    • 8
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 574-1020

    原理

    Glycine decarboxylase Antibody

    纯化方法

    Affinity purified

    免疫原

    A human recombinant partial protein (amino acids K574-S1020) was used as the immunogen for the Glycine decarboxylase antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the Glycine decarboxylase 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 Glycine decarboxylase 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

    GLDC (Glycine Dehydrogenase (GLDC))

    别名

    Glycine decarboxylase

    背景

    Glycine decarboxylase also known as glycine cleavage system P protein or glycine dehydrogenase is an enzyme that in humans is encoded by the GLDC gene. Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).

    UniProt

    P23378
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