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Syntrophin gamma 1 Protein (Myc-DYKDDDDK Tag)

SNTG1 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 ABIN2733135
发货至: 中国
  • 抗原 See all Syntrophin gamma 1 (SNTG1) 蛋白
    Syntrophin gamma 1 (SNTG1) (Syntrophin, gamma 1 (SNTG1))
    蛋白类型
    Recombinant
    宿主
    • 2
    • 1
    资源
    • 2
    • 1
    HEK-293 Cells
    标记
    This Syntrophin gamma 1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Syntrophin-4 / SNTG1 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 SNTG1 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
    Syntrophin gamma 1 (SNTG1) (Syntrophin, gamma 1 (SNTG1))
    别名
    Syntrophin-4,sntg1 (SNTG1 产品)
    别名
    SNTG1 Protein, G1SYN Protein, SYN4 Protein, 4933426D16Rik Protein, RGD1560290 Protein, syntrophin gamma 1 Protein, gamma-1-syntrophin Protein, syntrophin, gamma 1 Protein, SNTG1 Protein, sntg1 Protein, LOC100548083 Protein, Sntg1 Protein
    背景
    The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This family member plays a role in mediating gamma-enolase trafficking to the plasma membrane and in enhancing its neurotrophic activity. Mutations in this gene are associated with idiopathic scoliosis. Alternatively spliced transcript variants have been found for this gene.
    分子量
    57.8 kDa
    NCBI登录号
    NP_061840
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