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SCN8A 抗体

SCN8A 适用: 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7075647
发货至: 中国
  • 抗原 See all SCN8A 抗体
    SCN8A (Sodium Channel, Voltage-Gated, Type VIII, alpha (SCN8A))
    适用
    • 31
    • 25
    • 12
    • 5
    • 5
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    小鼠, 大鼠
    宿主
    • 29
    • 5
    克隆类型
    • 29
    • 5
    多克隆
    标记
    • 19
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SCN8A antibody is un-conjugated
    应用范围
    • 31
    • 13
    • 13
    • 13
    • 7
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    交叉反应
    大鼠
    纯化方法
    Affinity purification
    免疫原
    KLH conjugated Synthetic peptide corresponding to Mouse Nav1.6/SCN8A
    Top Product
    Discover our top product SCN8A Primary Antibody
  • 应用备注
    WB (M) 1:300-1:600, IHC/IF (M,R) 1:600-1:1200
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS, pH 7.4, 0.02 % sodium azide
    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
  • 抗原
    SCN8A (Sodium Channel, Voltage-Gated, Type VIII, alpha (SCN8A))
    别名
    Nav1.6/SCN8A (SCN8A 产品)
    别名
    CERIII antibody, CIAT antibody, EIEE13 antibody, MED antibody, NaCh6 antibody, Nav1.6 antibody, PN4 antibody, AI853486 antibody, C630029C19Rik antibody, dmu antibody, med antibody, mnd-2 antibody, mnd2 antibody, nmf2 antibody, nmf335 antibody, nmf58 antibody, nur14 antibody, seal antibody, sodium voltage-gated channel alpha subunit 8 antibody, sodium channel, voltage-gated, type VIII, alpha antibody, SCN8A antibody, Scn8a antibody
    背景
    This gene encodes a member of the sodium channel alpha subunit gene family. The encoded protein forms the ion pore region of the voltage-gated sodium channel. This protein is essential for the rapid membrane depolarization that occurs during the formation of the action potential in excitable neurons. Mutations in this gene are associated with cognitive disability, pancerebellar atrophy and ataxia. Alternate splicing results in multiple transcript variants.
    分子量
    225 kDa
    基因ID
    20273
    UniProt
    Q9WTU3
    途径
    Sensory Perception of Sound
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