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PGD 抗体 (AA 71-120)

The 兔 多克隆 anti-PGD antibody (ABIN1451001) specifically detects PGD in WB, ELISA, IF 和 IHC. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN1451001
发货至: 中国
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北京 101111
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Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for PGD 抗体 (AA 71-120) (ABIN1451001)

抗原

See all PGD 抗体
PGD (Phosphogluconate Dehydrogenase (PGD))

适用

  • 85
  • 43
  • 40
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 79
  • 6
兔

克隆类型

  • 57
  • 28
多克隆

标记

  • 34
  • 7
  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
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This PGD antibody is un-conjugated

应用范围

  • 69
  • 45
  • 31
  • 30
  • 27
  • 19
  • 13
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (IHC)
  • 抗原表位

    • 12
    • 12
    • 5
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 71-120

    原理

    PGD Antibody

    特异性

    PGD Polyclonal Antibody detects endogenous levels of PGD protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    免疫原

    The antiserum was produced against synthesized peptide derived from human PGD. AA range:71-120

    亚型

    IgG
  • 应用备注

    IHC: 100-300.WB 1:500 - 1:2000. ELISA: 1:5000.. IF 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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

    -20 °C

    储存方法

    Store at -20°C/1 year

    有效期

    12 months
  • 抗原

    PGD (Phosphogluconate Dehydrogenase (PGD))

    别名

    PGD

    背景

    Synonyms: PGD, PGDH, 6-phosphogluconate dehydrogenase, decarboxylating

    Background: 6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015],

    Gene Name: PGD

    Protein Name: 6-phosphogluconate dehydrogenase decarboxylating

    分子量

    53 kDa

    基因ID

    5226

    OMIM

    172200

    UniProt

    P52209
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