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DTD1 Protein (Myc-DYKDDDDK Tag)

DTD1 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 ABIN2722784
发货至: 中国
  • 抗原 See all DTD1 蛋白
    DTD1 (D-Tyrosyl-tRNA Deacylase 1 Homolog (S. Cerevisiae) (DTD1))
    蛋白类型
    Recombinant
    宿主
    • 5
    • 1
    • 1
    资源
    • 2
    • 1
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    • 1
    HEK-293 Cells
    标记
    This DTD1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Histidyl-tRNA synthetase 2 / HARS2 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 DTD1 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
    DTD1 (D-Tyrosyl-tRNA Deacylase 1 Homolog (S. Cerevisiae) (DTD1))
    别名
    Histidyl-Trna Synthetase 2,hars2 (DTD1 产品)
    别名
    0610006H08Rik Protein, Hars2 Protein, C20orf88 Protein, DUEB Protein, HARS2 Protein, bA379J5.3 Protein, bA555E18.1 Protein, pqn-68 Protein, hars2 Protein, zgc:92657 Protein, D-tyrosyl-tRNA deacylase 1 Protein, Dtd1 Protein, DTD1 Protein, dtd1 Protein
    背景
    Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is an enzyme belonging to the class II family of aminoacyl-tRNA synthetases. Functioning in the synthesis of histidyl-transfer RNA, the enzyme plays an accessory role in the regulation of protein biosynthesis. The gene is located in a head-to-head orientation with HARS on chromosome five, where the homologous genes likely share a bidirectional promoter. Mutations in this gene are associated with the pathogenesis of Perrault syndrome, which involves ovarian dysgenesis and sensorineural hearing loss. Alternative splicing results in multiple transcript variants of this gene.
    分子量
    53.3 kDa
    NCBI登录号
    NP_036340
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