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DLD 抗体 (Middle Region)

This anti-DLD antibody is a 兔 多克隆 antibody detecting DLD in WB. Suitable for 人 和 犬.
产品编号 ABIN631024
发货至: 中国

Quick Overview for DLD 抗体 (Middle Region) (ABIN631024)

抗原

See all DLD 抗体
DLD (Dihydrolipoamide Dehydrogenase (DLD))

适用

  • 50
  • 30
  • 29
  • 7
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
人, 犬

宿主

  • 58
  • 7

克隆类型

  • 54
  • 11
多克隆

标记

  • 43
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DLD antibody is un-conjugated

应用范围

  • 60
  • 29
  • 23
  • 18
  • 16
  • 13
  • 7
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 7
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    特异性

    DLD antibody was raised against the middle region of DLD

    纯化方法

    Affinity purified

    免疫原

    DLD antibody was raised using the middle region of DLD corresponding to a region with amino acids AGEMVNEAALALEYGASCEDIARVCHAHPTLSEAFREANLAASFGKSINF
  • 应用备注

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    说明

    DLD Blocking Peptide, , is also available for use as a blocking control in assays to test for specificity of this DLD antibody

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of DLD antibody in PBS

    浓度

    Lot specific

    缓冲液

    PBS

    注意事项

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    储存条件

    4 °C/-20 °C

    储存方法

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • 抗原

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    别名

    DLD

    背景

    DLD is the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.

    分子量

    56 kDa (MW of target protein)

    途径

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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