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ALDH6A1 抗体

This anti-ALDH6A1 antibody is a 兔 多克隆 antibody detecting ALDH6A1 in WB 和 IHC (p). Suitable for 人.
产品编号 ABIN2855626
发货至: 中国
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Quick Overview for ALDH6A1 抗体 (ABIN2855626)

抗原

See all ALDH6A1 抗体
ALDH6A1 (Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))

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 ALDH6A1 antibody is un-conjugated

应用范围

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

    人, 小鼠

    产品特性

    Rabbit Polyclonal antibody to ALDH6A1 (aldehyde dehydrogenase 6 family, member A1)
    ALDH6A1 antibody

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human ALDH6A1. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

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

    说明

    Positive Control: Mouse liver , HepG2

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 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

    ALDH6A1 (Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))

    别名

    aldehyde dehydrogenase 6 family member A1

    背景

    This protein belongs to the aldehyde dehydrogenases family of proteins. This enzyme plays a role in the valine and pyrimidine catabolic pathways. The product of this gene, a mitochondrial methylmalonate semialdehyde dehydrogenase, catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids.

    Cellular Localization: Mitochondrion

    分子量

    58 kDa

    基因ID

    4329

    UniProt

    Q02252

    途径

    Brown Fat Cell Differentiation
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