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OSTM1 Protein (Myc-DYKDDDDK Tag)

OSTM1 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 ABIN2728027
发货至: 中国
  • 抗原 See all OSTM1 蛋白
    OSTM1 (Osteopetrosis Associated Transmembrane Protein 1 (OSTM1))
    蛋白类型
    Recombinant
    宿主
    • 5
    • 3
    • 1
    资源
    • 4
    • 3
    • 1
    • 1
    HEK-293 Cells
    标记
    This OSTM1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human OSTM1 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 OSTM1 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
    OSTM1 (Osteopetrosis Associated Transmembrane Protein 1 (OSTM1))
    别名
    Ostm1 (OSTM1 产品)
    别名
    MGC145644 Protein, si:ch73-257c13.3 Protein, GIPN Protein, GL Protein, OPTB5 Protein, 1200002H13Rik Protein, HSPC019 Protein, gl Protein, Gipn Protein, OSTM1 Protein, osteopetrosis associated transmembrane protein 1 Protein, OSTM1 Protein, ostm1 Protein, Ostm1 Protein
    背景
    This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis.
    分子量
    37.1 kDa
    NCBI登录号
    NP_054747
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