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Glycogen Synthase 2 抗体 (AA 594-703)

GYS2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6141549
发货至: 中国
  • 抗原 See all Glycogen Synthase 2 (GYS2) 抗体
    Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
    抗原表位
    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 594-703
    适用
    • 19
    • 17
    • 14
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    宿主
    • 27
    • 2
    克隆类型
    • 27
    • 2
    多克隆
    标记
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Glycogen Synthase 2 antibody is un-conjugated
    应用范围
    • 21
    • 13
    • 13
    • 7
    • 3
    • 3
    • 1
    Western Blotting (WB)
    序列
    DLLDWRYLGR YYQHARHLTL SRAFPDKFHV ELTSPPTTEG FKYPRPSSVP PSPSGSQASS PQSSDVEDEV EDERYDEEEE AERDRLNIKS PFSLSHVPHG KKKLHGEYKN
    交叉反应
    小鼠
    产品特性
    Polyclonal Antibodies
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 594-703 of human GYS2 (NP_068776.2).
    亚型
    IgG
    Top Product
    Discover our top product GYS2 Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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
    Glycogen Synthase 2 (GYS2) (Glycogen Synthase 2, Liver (GYS2))
    别名
    GYS2 (GYS2 产品)
    别名
    cb765 antibody, zgc:112057 antibody, BC021322 antibody, LGS antibody, GLYSN antibody, glycogen synthase 2 antibody, gys2 antibody, Gys2 antibody, GYS2 antibody
    背景
    The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content.,GYS2,Cancer,Signal Transduction,PI3K-Akt Signaling Pathway,Cell Biology & Developmental Biology,Cytoskeleton,Actins,Endocrine & Metabolism,Carbohydrate metabolism,AMPK Signaling Pathway,Insulin Receptor Signaling Pathway,GYS2
    分子量
    80 kDa
    基因ID
    2998
    UniProt
    P54840
    途径
    AMPK Signaling, Cellular Glucan Metabolic Process
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