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TM4SF20 Protein (Myc-DYKDDDDK Tag)

TM4SF20 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 ABIN2733827
发货至: 中国
  • 抗原 See all TM4SF20 products
    TM4SF20 (Transmembrane 4 L Six Family Member 20 (TM4SF20))
    蛋白类型
    Recombinant
    宿主
    • 1
    • 1
    资源
    • 2
    HEK-293 Cells
    标记
    This TM4SF20 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human TM4SF20 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • 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
    TM4SF20 (Transmembrane 4 L Six Family Member 20 (TM4SF20))
    别名
    Tm4sf20 (TM4SF20 产品)
    别名
    pro994 Protein, tcce518 Protein, PRO994 Protein, TCCE518 Protein, 1810018L02Rik Protein, transmembrane 4 L six family member 20 Protein, transmembrane 4 L six family member 20 L homeolog Protein, TM4SF20 Protein, Tm4sf20 Protein, tm4sf20.L Protein, tm4sf20 Protein
    背景
    The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5.
    分子量
    24.9 kDa
    NCBI登录号
    NP_079071
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