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ATP7A 抗体

ATP7A 适用: 人, 大鼠 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7264427
发货至: 中国
  • 抗原 See all ATP7A 抗体
    ATP7A (ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A))
    适用
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    人, 大鼠
    宿主
    • 35
    • 14
    • 1
    • 1
    克隆类型
    • 37
    • 14
    多克隆
    标记
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    This ATP7A antibody is un-conjugated
    应用范围
    • 42
    • 18
    • 14
    • 13
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    • 13
    • 11
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    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human ATP7A (NP_000043.4).
    亚型
    IgG
    Top Product
    Discover our top product ATP7A Primary Antibody
  • 应用备注
    IHC 1:50-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    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
    ATP7A (ATPase, Cu++ Transporting, alpha Polypeptide (ATP7A))
    别名
    ATP7A (ATP7A 产品)
    别名
    ATP7A antibody, cal antibody, wu:fc43e01 antibody, zgc:153422 antibody, zgc:158633 antibody, DDBDRAFT_0218568 antibody, DDBDRAFT_0235190 antibody, DDB_0218568 antibody, DDB_0235190 antibody, atpase antibody, Atp7a antibody, kal antibody, atp7a antibody, DSMAX antibody, MK antibody, MNK antibody, SMAX3 antibody, Blo antibody, DXHXS1608e antibody, I14 antibody, Mo antibody, blotchy antibody, br antibody, brindled antibody, mottled antibody, Mnk antibody, ATPase copper transporting alpha antibody, ATPase, Cu++ transporting, alpha polypeptide antibody, P-type ATPase antibody, ATP synthase subunit a antibody, copper-transporting ATPase 1 antibody, ATP7A antibody, atp7a antibody, LOC100049514 antibody, Atp7a antibody, LOC412379 antibody
    背景
    This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed.
    基因ID
    538
    UniProt
    Q04656
    途径
    Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process
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