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Gephyrin Protein (GPHN) (Transcript Variant 1) (Myc-DYKDDDDK Tag)

GPHN 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2721820
发货至: 中国
  • 抗原 See all Gephyrin (GPHN) 蛋白
    Gephyrin (GPHN)
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 2
    • 1
    资源
    • 2
    • 1
    HEK-293 Cells
    标记
    This Gephyrin protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Gephyrin (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product GPHN 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    Gephyrin (GPHN)
    别名
    Gephyrin (GPHN 产品)
    别名
    5730552E08Rik Protein, AI662856 Protein, BC027112 Protein, C230040D23 Protein, GPH Protein, GPHRYN Protein, geph Protein, Geph Protein, GPHN Protein, GEPH Protein, HKPX1 Protein, gpgb1 Protein, DKFZp459M0825 Protein, gephyrin Protein, gephyrin L homeolog Protein, gephyrin a Protein, Gphn Protein, GPHN Protein, gphn.L Protein, gphna Protein, PTRG_08978 Protein, VDBG_00775 Protein, Tsp_03043 Protein, gphn Protein
    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
    NCBI登录号
    NP_065857
    途径
    Synaptic Membrane, Skeletal Muscle Fiber Development
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