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PYGM 抗体

PYGM 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7241813
发货至: 中国
  • 抗原 See all PYGM 抗体
    PYGM (Phosphorylase, Glycogen, Muscle (PYGM))
    适用
    • 31
    • 21
    • 18
    • 6
    • 4
    • 4
    • 4
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    • 1
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 45
    • 6
    • 2
    克隆类型
    • 47
    • 6
    多克隆
    标记
    • 23
    • 7
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PYGM antibody is un-conjugated
    应用范围
    • 44
    • 16
    • 16
    • 13
    • 13
    • 11
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human PYGM
    亚型
    IgG
    Top Product
    Discover our top product PYGM Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:30-1:150
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.4 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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. Avoid freeze / thaw cycles.
  • 抗原
    PYGM (Phosphorylase, Glycogen, Muscle (PYGM))
    别名
    PYGM (PYGM 产品)
    别名
    pygb antibody, im:7150327 antibody, zgc:110706 antibody, AI115133 antibody, PG antibody, Muscpho antibody, zgc:63642 antibody, phosphorylase, glycogen, muscle L homeolog antibody, glycogen phosphorylase, muscle associated antibody, phosphorylase, glycogen, muscle A antibody, glycogen phosphorylase, muscle form antibody, muscle glycogen phosphorylase antibody, phosphorylase, glycogen, muscle b antibody, pygm.L antibody, PYGM antibody, pygma antibody, THA_70 antibody, Pygm antibody, pygmb antibody
    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
    UniProt
    P11217
    途径
    Cellular Glucan Metabolic Process
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