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GLDC 抗体 (N-Term)

This anti-GLDC antibody is a 兔 多克隆 antibody detecting GLDC in WB. Suitable for 人 和 小鼠.
产品编号 ABIN653448
发货至: 中国
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Quick Overview for GLDC 抗体 (N-Term) (ABIN653448)

抗原

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

适用

  • 44
  • 14
  • 3
人, 小鼠

宿主

  • 45
  • 1

克隆类型

  • 45
  • 1
多克隆

标记

  • 20
  • 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

  • 42
  • 15
  • 13
  • 13
  • 13
  • 9
  • 7
  • 5
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

克隆位点

RB23981
  • 抗原表位

    • 15
    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 49-77, N-Term

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This GLDC antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 49-77 amino acids from the N-terminal region of human GLDC.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000. WB: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: 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

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    GLDC (Glycine Dehydrogenase (GLDC))

    别名

    GLDC

    背景

    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 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).

    分子量

    112730

    基因ID

    2731

    NCBI登录号

    NP_000161

    UniProt

    P23378
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