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ALDH4A1 抗体

This anti-ALDH4A1 antibody is a 兔 多克隆 antibody detecting ALDH4A1 in WB, IHC 和 ELISA. Suitable for 人, 小鼠, 犬 和 斑马鱼.
产品编号 ABIN2462884
发货至: 中国

Quick Overview for ALDH4A1 抗体 (ABIN2462884)

抗原

See all ALDH4A1 抗体
ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

适用

  • 26
  • 10
  • 10
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人, 小鼠, 犬, 斑马鱼

宿主

  • 21
  • 5

克隆类型

  • 24
  • 2
多克隆

标记

  • 26
This ALDH4A1 antibody is un-conjugated

应用范围

  • 26
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Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • 纯化方法

    Antibody is purified by protein A chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ALDH4A1.
  • 应用备注

    ALDH4A1 antibody can be used for detection of ALDH4A1 by ELISA at 1:312500. ALDH4A1 antibody can be used for detection of ALDH4A1 by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store ALDH4A1 antibody at -20 °C.
  • 抗原

    ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

    别名

    ALDH4A1

    背景

    ALDH4A1 belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline.This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Two transcript variants encoding the same protein have been identified for this gene.

    分子量

    62 kDa, 62 kDa

    基因ID

    8659

    NCBI登录号

    NP_003739

    UniProt

    P30038

    途径

    Monocarboxylic Acid Catabolic Process
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