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Gephyrin 抗体

GPHN 适用: 人 WB 宿主: 兔 Monoclonal unconjugated
产品编号 ABIN7267375
发货至: 中国
  • 抗原 See all Gephyrin (GPHN) 抗体
    Gephyrin (GPHN)
    适用
    • 51
    • 34
    • 26
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    宿主
    • 47
    • 5
    • 1
    • 1
    克隆类型
    • 43
    • 11
    单克隆
    标记
    • 27
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This Gephyrin antibody is un-conjugated
    应用范围
    • 35
    • 19
    • 17
    • 16
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    原理
    Gephyrin Rabbit mAb
    交叉反应
    人, 小鼠, 大鼠
    产品特性
    Monoclonal Antibodies
    纯化方法
    Affinity purification
    免疫原
    A synthesized peptide derived from human Gephyrin
    亚型
    IgG
    Top Product
    Discover our top product GPHN Primary Antibody
  • 应用备注
    WB,1:500 - 1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
    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
    Gephyrin (GPHN)
    别名
    GPHN (GPHN 产品)
    别名
    5730552E08Rik antibody, AI662856 antibody, BC027112 antibody, C230040D23 antibody, GPH antibody, GPHRYN antibody, geph antibody, Geph antibody, GPHN antibody, GEPH antibody, HKPX1 antibody, gpgb1 antibody, DKFZp459M0825 antibody, gephyrin antibody, gephyrin L homeolog antibody, gephyrin a antibody, Gphn antibody, GPHN antibody, gphn.L antibody, gphna antibody, PTRG_08978 antibody, VDBG_00775 antibody, Tsp_03043 antibody, gphn antibody
    背景
    This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described, however, the full-length nature of all transcript variants is not currently known. [provided by RefSeq, Jul 2008],GEPH, GPH, GPHRYN, HKPX1, MOCODC,Cell Adhesion,Cell Biology & Developmental Biology,Cytoskeleton_Microtubules,Neuroscience,GPHN
    分子量
    93kDa
    基因ID
    10243
    UniProt
    Q9NQX3
    途径
    Synaptic Membrane, Skeletal Muscle Fiber Development
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