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AMPD1 抗体 (AA 5-747) (HRP)

The 兔 多克隆 anti-AMPD1 antibody is suitable to detect AMPD1 in samples from 人, 小鼠 和 大鼠. It has been validated for ELISA, WB 和 IHC.
产品编号 ABIN7966733
发货至: 中国
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for AMPD1 抗体 (AA 5-747) (HRP) (ABIN7966733)

抗原

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

适用

  • 42
  • 35
  • 35
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
人, 小鼠, 大鼠

宿主

  • 49
  • 1

克隆类型

  • 50
多克隆

标记

  • 17
  • 4
  • 3
  • 2
  • 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 conjugated to HRP

应用范围

  • 17
  • 14
  • 13
  • 13
  • 11
  • 7
  • 5
  • 3
  • 2
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

    • 15
    • 12
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 5-747

    原理

    Anti-AMPD1 Antibody HRP Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins

    预测反应

    Human AMPD1 shares 92.7% amino acid (aa) sequence identity with both mouse,rat AMPD1.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human AMPD1 recombinant protein (Position: K5-E747). Human AMPD1 shares 92.7% amino acid (aa) sequence identity with both mouse and rat AMPD1.

    亚型

    IgG
  • 应用备注

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

    别名

    AMPD1

    背景

    Background: AMP deaminase 1 is an enzyme that in humans is encoded by the AMPD1 gene. 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.

    Gene Full Name: adenosine monophosphate deaminase 1

    基因ID

    270

    UniProt

    P23109
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