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KCNK9 抗体

KCNK9 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7243493
发货至: 中国
  • 抗原 See all KCNK9 抗体
    KCNK9 (Potassium Channel, Subfamily K, Member 9 (KCNK9))
    适用
    • 39
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    宿主
    • 41
    • 9
    克隆类型
    • 41
    • 9
    多克隆
    标记
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    This KCNK9 antibody is un-conjugated
    应用范围
    • 39
    • 15
    • 13
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    • 6
    • 4
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    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human KCNK9
    亚型
    IgG
    Top Product
    Discover our top product KCNK9 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:100-1:300
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.4 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
    KCNK9 (Potassium Channel, Subfamily K, Member 9 (KCNK9))
    别名
    KCNK9 (KCNK9 产品)
    别名
    Task3 antibody, K2p9.1 antibody, KT3.2 antibody, TASK-3 antibody, TASK3 antibody, KCNK9 antibody, LOC799704 antibody, Kcnk9 antibody, task3 antibody, k2p9.1 antibody, task-3 antibody, kt3.2 antibody, potassium channel, subfamily K, member 9 antibody, potassium two pore domain channel subfamily K member 9 antibody, potassium channel, two pore domain subfamily K, member 9 antibody, potassium channel, two pore domain subfamily K, member 9 L homeolog antibody, Kcnk9 antibody, KCNK9 antibody, kcnk9 antibody, kcnk9.L antibody
    背景
    This gene encodes a protein that contains multiple transmembrane regions and two pore-forming P domains and functions as a pH -dependent potassium channel. Amplification and overexpression of this gene have been observed in several types of human carcinomas. This gene is imprinted in the brain, with preferential expression from the maternal allele. A mutation in this gene was associated with Birk-Barel mental retardation dysmorphism syndrome. Alternative splicing results in multiple transcript variants.
    分子量
    42 kDa
    NCBI登录号
    NP_001269463
    UniProt
    Q9NPC2
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