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PYGM 抗体 (AA 390-804) (HRP)

This 兔 多克隆 antibody specifically detects PYGM in WB, IHC 和 ELISA. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN8022440
发货至: 中国
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Quick Overview for PYGM 抗体 (AA 390-804) (HRP) (ABIN8022440)

抗原

See all PYGM 抗体
PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

适用

  • 44
  • 33
  • 31
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 57
  • 7

克隆类型

  • 57
  • 7
多克隆

标记

  • 26
  • 7
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PYGM antibody is conjugated to HRP

应用范围

  • 47
  • 19
  • 18
  • 13
  • 13
  • 12
  • 9
  • 3
  • 3
  • 3
  • 2
  • 2
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • 抗原表位

    • 15
    • 11
    • 8
    • 6
    • 3
    • 2
    • 1
    • 1
    AA 390-804

    原理

    Anti-PYGM Antibody HRP Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins

    预测反应

    Human PYGMshares 95.9%,94.2% amino acid (aa) sequence identity with mouse,rat PYGM,respectively.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human PYGM recombinant protein (Position: V390-R804). Human PYGMshares 95.9% and 94.2% amino acid (aa) sequence identity with mouse and rat PYGM, respectively.

    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

    PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

    别名

    PYGM

    背景

    Background: This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.

    Gene Full Name: glycogen phosphorylase, muscle associated

    基因ID

    5837

    UniProt

    P11217

    途径

    Cellular Glucan Metabolic Process
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