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POMT1 抗体

POMT1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6566852
发货至: 中国
  • 抗原 See all POMT1 抗体
    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))
    适用
    • 42
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 43
    克隆类型
    • 43
    多克隆
    标记
    • 17
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This POMT1 antibody is un-conjugated
    应用范围
    • 28
    • 19
    • 17
    • 16
    • 13
    • 13
    • 7
    • 3
    • 2
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human POMT1
    亚型
    IgG
    Top Product
    Discover our top product POMT1 Primary Antibody
  • 应用备注
    WB 1:1000 - 1:2000
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: 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
    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))
    别名
    POMT1 (POMT1 产品)
    别名
    LGMD2K antibody, MDDGA1 antibody, MDDGB1 antibody, MDDGC1 antibody, RT antibody, AI505244 antibody, protein O-mannosyltransferase 1 antibody, protein-O-mannosyltransferase 1 antibody, POMT1 antibody, Pomt1 antibody
    背景

    Synonyms: Dolichyl phosphate mannose protein mannosyltransferase 1,Dolichyl phosphate mannose protein mannosyltransferase1,Dolichyl-phosphate-mannose--protein mannosyltransferase 1,LGMD2K,MDDGA1,MDDGB1,MDDGC1,POMT 1,POMT1,POMT1,Protein O mannosyl transferase 1,Protein O mannosyl transferase1,Protein O-mannosyl-transferase 1,Rotate abdomen,Drosophila,homolog of,RT

    Background: The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.

    分子量

    Observed_MW: 53kDa

    Calculated_MW: 69kDa/76kDa/82kDa/84kDa

    基因ID
    10585
    UniProt
    Q9Y6A1
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