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AMPD1 抗体 (AA 261-310)

This 兔 多克隆 antibody specifically detects AMPD1 in ELISA, IHC 和 IF. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN1534626
发货至: 中国
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Quick Overview for AMPD1 抗体 (AA 261-310) (ABIN1534626)

抗原

See all AMPD1 抗体
AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

适用

  • 40
  • 33
  • 18
  • 2
  • 2
  • 2
  • 2
  • 1
人, 小鼠, 大鼠

宿主

  • 47
  • 1
兔

克隆类型

  • 48
多克隆

标记

  • 14
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This AMPD1 antibody is un-conjugated

应用范围

  • 22
  • 21
  • 15
  • 13
  • 13
  • 11
  • 3
  • 3
  • 2
ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
  • 抗原表位

    • 15
    • 13
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 261-310

    原理

    AMPD1 Antibody

    特异性

    AMPD1 Polyclonal Antibody detects endogenous levels of AMPD1 protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    纯度

    > 95 %

    免疫原

    The antiserum was produced against synthesized peptide derived from human AMPD1. AA range:261-310

    亚型

    IgG
  • 应用备注

    IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

    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.

    储存条件

    -20 °C

    储存方法

    Store at -20°C/1 year

    有效期

    12 months
  • 抗原

    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

    别名

    AMPD1

    背景

    Synonyms: AMPD1, AMP deaminase 1, AMP deaminase isoform M, Myoadenylate deaminase

    Background: Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010],

    Gene Name: AMPD1

    Protein Name: AMP deaminase 1

    分子量

    86 kDa

    基因ID

    270

    OMIM

    102770

    UniProt

    P23109
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