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Glucose-6-Phosphate Dehydrogenase 抗体

This anti-Glucose-6-Phosphate Dehydrogenase antibody is a 兔 多克隆 antibody detecting Glucose-6-Phosphate Dehydrogenase in WB, ELISA 和 IHC (p). Suitable for 人.
产品编号 ABIN7466699
发货至: 中国

Quick Overview for Glucose-6-Phosphate Dehydrogenase 抗体 (ABIN7466699)

抗原

See all Glucose-6-Phosphate Dehydrogenase (G6PD) 抗体
Glucose-6-Phosphate Dehydrogenase (G6PD)

适用

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宿主

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克隆类型

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多克隆

标记

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This Glucose-6-Phosphate Dehydrogenase antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 交叉反应

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human G6PD. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. ELISA: 1:1000-1:10000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: Molt-4

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.01 mg/mL

    缓冲液

    0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): 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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    Glucose-6-Phosphate Dehydrogenase (G6PD)

    别名

    glucose-6-phosphate dehydrogenase

    背景

    Glucose-6-phosphate dehydrogenase , G6PD1,This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]

    分子量

    59 kDa

    基因ID

    2539

    UniProt

    P11413

    途径

    Regulation of Systemic Arterial Blood Pressure by Hormones
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