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ALDH4A1 抗体 (N-Term)

This anti-ALDH4A1 antibody is a 兔 多克隆 antibody detecting ALDH4A1 in WB 和 IHC. Suitable for 人, 小鼠, 大鼠, Cow, 犬, 马, 兔, 豚鼠 和 Pig.
产品编号 ABIN2782323
发货至: 中国

Quick Overview for ALDH4A1 抗体 (N-Term) (ABIN2782323)

抗原

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

适用

  • 26
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人, 小鼠, 大鼠, Cow, 犬, 马, 兔, 豚鼠, Pig

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

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Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

    • 6
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    • 1
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    • 1
    N-Term

    序列

    QGKTVIQAEI DAAAELIDFF RFNAKYAVEL EGQQPISVPP STNSTVYRGL

    预测反应

    Cow: 86%, Dog: 93%, Guinea Pig: 85%, Horse: 100%, Human: 100%, Mouse: 92%, Pig: 100%, Rabbit: 92%, Rat: 92%

    产品特性

    This is a rabbit polyclonal antibody against ALDH4A1. It was validated on Western Blot and immunohistochemistry.

    纯化方法

    Protein A purified

    免疫原

    The immunogen is a synthetic peptide directed towards the N terminal region of human ALDH4A1
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 214 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 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.
    Alias Symbols: RP11-128M10.1, ALDH4, P5CD, P5CDh, P5CDhL, P5CDhS
    Protein Interaction Partner: UBC, MDM2, ALDH4A1, ARG1, APP,
    Protein Size: 214

    分子量

    24 kDa

    基因ID

    8659

    NCBI登录号

    NM_001161504

    UniProt

    Q5TF55

    途径

    Monocarboxylic Acid Catabolic Process
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