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KCTD7 抗体

KCTD7 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7245461
发货至: 中国
  • 抗原 See all KCTD7 抗体
    KCTD7 (Potassium Channel Tetramerisation Domain Containing 7 (KCTD7))
    适用
    • 31
    • 10
    • 10
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    人, 大鼠, 小鼠
    宿主
    • 29
    • 2
    克隆类型
    • 31
    多克隆
    标记
    • 11
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This KCTD7 antibody is un-conjugated
    应用范围
    • 20
    • 18
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of human KCTD7
    亚型
    IgG
  • 应用备注
    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1.56 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
    KCTD7 (Potassium Channel Tetramerisation Domain Containing 7 (KCTD7))
    别名
    KCTD7 (KCTD7 产品)
    别名
    4932409E18 antibody, 9430010P06Rik antibody, zgc:136884 antibody, CLN14 antibody, EPM3 antibody, potassium channel tetramerization domain containing 7 antibody, potassium channel tetramerisation domain containing 7 antibody, KCTD7 antibody, Kctd7 antibody, kctd7 antibody
    背景
    KCTD7 (Potassium Channel Tetramerization Domain Containing 7) is a Protein Coding gene. Diseases associated with KCTD7 include Epilepsy, Progressive Myoclonic 3, With Or Without Intracellular Inclusions and Cln14 Disease. Among its related pathways are Neuropathic Pain-Signaling in Dorsal Horn Neurons and Innate Immune System. An important paralog of this gene is KCTD14. This gene encodes a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.
    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 33 kDa

    UniProt
    Q96MP8
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