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Monoamine Oxidase A 抗体

This anti-Monoamine Oxidase A antibody is a 兔 多克隆 antibody detecting Monoamine Oxidase A in WB 和 ELISA. Suitable for 人, 小鼠, 大鼠 和 犬.
产品编号 ABIN2463952
发货至: 中国

Quick Overview for Monoamine Oxidase A 抗体 (ABIN2463952)

抗原

See all Monoamine Oxidase A (MAOA) 抗体
Monoamine Oxidase A (MAOA)

适用

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人, 小鼠, 大鼠, 犬

宿主

  • 55
  • 8
  • 1

克隆类型

  • 53
  • 11
多克隆

标记

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This Monoamine Oxidase A antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by peptide affinity chromatography method.

    免疫原

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

    MAOA antibody can be used for detection of MAOA by ELISA at 1:1562500. MAOA antibody can be used for detection of MAOA by western blot at 1 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 50 ?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 MAOA antibody at -20 °C.
  • 抗原

    Monoamine Oxidase A (MAOA)

    别名

    MAOA

    背景

    MAOA catalyzes the oxidative deamination of biogenic and xenobiotic amines and has important functions in the metabolism of neuroactive and vasoactive amines in the central nervous system and peripheral tissues. MAOA preferentially oxidizes biogenic amines such as 5-hydroxytryptamine (5-HT), norepinephrine and epinephrine.This gene encodes monoamine oxidase A, an enzyme that degrades amine neurotransmitters, such as dopamine, norepinephrine, and serotonin. The protein localizes to the mitochondrial outer membrane. The gene is adjacent to a related gene on the opposite strand of chromosome X. Mutation in this gene results in monoamine oxidase deficiency, or Brunner syndrome.

    分子量

    60 kDa

    基因ID

    4128

    NCBI登录号

    NP_000231

    UniProt

    P21397
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