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Gephyrin 抗体

GPHN 适用: 人 WB, IHC, FACS 宿主: 小鼠 Monoclonal 3C6 unconjugated
产品编号 ABIN2721814
发货至: 中国
  • 抗原 See all Gephyrin (GPHN) 抗体
    Gephyrin (GPHN)
    适用
    • 52
    • 34
    • 26
    • 4
    • 4
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    • 4
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    • 3
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    宿主
    • 48
    • 5
    • 1
    • 1
    小鼠
    克隆类型
    • 43
    • 12
    单克隆
    标记
    • 28
    • 5
    • 3
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    This Gephyrin antibody is un-conjugated
    应用范围
    • 36
    • 19
    • 17
    • 16
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)
    产品特性
    Homo sapiens gephyrin (GPHN), transcript variant 1
    纯化方法
    Purified from mouse ascites fluids by affinity chromatography
    免疫原
    Full length human recombinant protein of human GPHN (NP_065857) produced in HEK293T cell.
    克隆位点
    3C6
    亚型
    IgG2a
    Top Product
    Discover our top product GPHN Primary Antibody
  • 应用备注
    WB 1:1000~2000, IHC 1:150, FLOW 1:100
    说明

    The concentration of the product may vary between diferrent lots.

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.5-1.0 mg/mL
    缓冲液
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 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
    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.
    分子量
    83.3 kDa
    基因ID
    10243
    NCBI登录号
    NM_020806
    HGNC
    10243
    途径
    Synaptic Membrane, Skeletal Muscle Fiber Development
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