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ABCB6 抗体

ABCB6 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2428945
发货至: 中国
  • 抗原 See all ABCB6 抗体
    ABCB6 (ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 6 (ABCB6))
    适用
    • 28
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    人, 小鼠, 大鼠
    宿主
    • 26
    • 2
    克隆类型
    • 27
    • 1
    多克隆
    标记
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    • 1
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    This ABCB6 antibody is un-conjugated
    应用范围
    • 13
    • 13
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    • 5
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    • 1
    Western Blotting (WB), ELISA
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human ABCB6
    亚型
    IgG
    Top Product
    Discover our top product ABCB6 Primary Antibody
  • 应用备注
    WB 1:200-1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.1 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
    Avoid freeze / thaw cycles.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    ABCB6 (ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 6 (ABCB6))
    别名
    ABCB6 (ABCB6 产品)
    别名
    ABCB6 antibody, abcb6 antibody, ABC antibody, ABC14 antibody, LAN antibody, MCOPCB7 antibody, MTABC3 antibody, PRP antibody, umat antibody, 1200005B17Rik antibody, ATP binding cassette subfamily B member 6 (Langereis blood group) antibody, ATP binding cassette subfamily B member 6 antibody, ATP-binding cassette, sub-family B (MDR/TAP), member 6a antibody, ATP-binding cassette, sub-family B (MDR/TAP), member 6 antibody, ABCB6 antibody, abcb6a antibody, abcb6 antibody, Abcb6 antibody
    背景
    The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This half-transporter likely plays a role in mitochondrial function. Localized to 2q26, this gene is considered a candidate gene for lethal neonatal metabolic syndrome, a disorder of mitochondrial function.
    分子量
    Calculated MW: 94 kDa
    途径
    Transition Metal Ion Homeostasis
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