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KCNT1 抗体

KCNT1 适用: 人, 大鼠, 小鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7251640
发货至: 中国
  • 抗原 See all KCNT1 抗体
    KCNT1 (Potassium Channel, Subfamily T, Member 1 (KCNT1))
    适用
    • 35
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    人, 大鼠, 小鼠
    宿主
    • 35
    • 12
    克隆类型
    • 35
    • 12
    多克隆
    标记
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    This KCNT1 antibody is un-conjugated
    应用范围
    • 34
    • 16
    • 13
    • 13
    • 11
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    Immunohistochemistry (IHC), ELISA
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of human KCNT1
    亚型
    IgG
    Top Product
    Discover our top product KCNT1 Primary Antibody
  • 应用备注
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.9 mg/mL
    缓冲液
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    KCNT1 (Potassium Channel, Subfamily T, Member 1 (KCNT1))
    别名
    KCNT1 (KCNT1 产品)
    别名
    EIEE14 antibody, ENFL5 antibody, KCa4.1 antibody, SLACK antibody, bA100C15.2 antibody, Slack antibody, rSlo2 antibody, C030030G16Rik antibody, mKIAA1422 antibody, slo2 antibody, slack antibody, Slo2.2 antibody, MGC146594 antibody, potassium sodium-activated channel subfamily T member 1 antibody, potassium channel subfamily T member 1 antibody, potassium channel, subfamily T, member 1 antibody, potassium channel, sodium activated subfamily T, member 1 antibody, KCNT1 antibody, LOC100436526 antibody, Kcnt1 antibody, kcnt1 antibody
    背景
    Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants.
    UniProt
    Q5JUK3
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