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PRODH 抗体 (Center)

The 兔 多克隆 anti-PRODH antibody is suitable to detect PRODH in samples from 人. It has been validated for WB.
产品编号 ABIN2855390
发货至: 中国
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Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for PRODH 抗体 (Center) (ABIN2855390)

抗原

See all PRODH 抗体
PRODH (Proline Dehydrogenase (Oxidase) 1 (PRODH))

适用

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宿主

  • 45
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克隆类型

  • 47
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多克隆

标记

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This PRODH antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    Center

    交叉反应

    小鼠, 大鼠, 牛

    交叉反应 (详细)

    Mouse (84 %), Rat (83 %), Bovine (80 %)

    产品特性

    Rabbit Polyclonal antibody to PRODH (proline dehydrogenase (oxidase) 1)
    PRODH antibody [N1N3]

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

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

    亚型

    IgG
  • 应用备注

    Suggested dilution Reference Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceWestern blot1:500-1:3000*

    说明

    Positive Control: 293T

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1XPBS, 1 % BSA, 20 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

    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

    -20 °C

    储存方法

    Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    PRODH (Proline Dehydrogenase (Oxidase) 1 (PRODH))

    别名

    PRODH

    背景

    The protein encoded by this gene is a mitochondrial proline dehydrogenase that catalyzes the first step in proline degradation. Defects in this gene are a cause of hyperprolinemia type 1 and possibly susceptibility to schizophrenia 4 (SCZD4). The gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes DiGeorge syndrome and CATCH22 syndrome.

    Cellular Localization: Mitochondrion matrix

    分子量

    68 kDa

    基因ID

    5625

    途径

    Response to Water Deprivation, Monocarboxylic Acid Catabolic Process
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