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PYGM 抗体 (AA 390-804)

This 兔 多克隆 anti-PYGM antibody specifically detects PYGM in WB, IHC, ELISA 和 FACS. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7825691
发货至: 中国
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Quick Overview for PYGM 抗体 (AA 390-804) (ABIN7825691)

抗原

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

适用

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人, 小鼠, 大鼠

宿主

  • 46
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克隆类型

  • 46
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多克隆

标记

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This PYGM antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)
  • 抗原表位

    • 15
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    • 1
    • 1
    AA 390-804

    原理

    Anti-PYGM Antibody

    交叉反应 (详细)

    No cross-reactivity with other proteins

    产品特性

    Anti-PYGM Antibody catalog # A02971-1. Tested in WB, IHC, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

    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, 0.25-0.5 μg/mL, Mouse, Rat
    Immunohistochemistry, 2-5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    浓度

    500 μg/mL

    缓冲液

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    储存条件

    4 °C,-20 °C

    储存方法

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • 抗原

    PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

    别名

    PYGM

    背景

    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.

    分子量

    97 kDa

    基因ID

    5837

    UniProt

    P11217

    途径

    Cellular Glucan Metabolic Process
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