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OAT 抗体

This anti-OAT antibody is a 兔 多克隆 antibody detecting OAT in WB, IF, ICC 和 IHC (p). Suitable for 人.
产品编号 ABIN2855721
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for OAT 抗体 (ABIN2855721)

抗原

See all OAT 抗体
OAT (Ornithine Aminotransferase (OAT))

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 OAT antibody is un-conjugated

应用范围

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

    人, 小鼠

    产品特性

    Rabbit Polyclonal antibody to OAT (ornithine aminotransferase)
    OAT antibody [N1C3]

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

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

    亚型

    IgG
  • 应用备注

    WB: 1:1000-1:10000. ICC/IF: 1:100-1:1000. 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 brain , K562 , THP-1 , OAT-transfected 293T

    Validation: Overexpression

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.28 mg/mL

    缓冲液

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.025 % ProClin 300

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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

    OAT (Ornithine Aminotransferase (OAT))

    别名

    ornithine aminotransferase

    背景

    This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme is the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy.

    Cellular Localization: Mitochondrion matrix

    分子量

    49 kDa

    基因ID

    4942

    UniProt

    P04181
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