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TRMU Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

TRMU 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 ABIN2734365
发货至: 中国
  • 抗原 See all TRMU 蛋白
    TRMU (tRNA 5-Methylaminomethyl-2-Thiouridylate Methyltransferase (TRMU))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 2
    • 1
    • 1
    • 1
    资源
    • 2
    • 2
    • 1
    HEK-293 Cells
    标记
    This TRMU protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human TRMU / TRMT1 (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 TRMU 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
    TRMU (tRNA 5-Methylaminomethyl-2-Thiouridylate Methyltransferase (TRMU))
    别名
    Trmu,trmt1 (TRMU 产品)
    别名
    MTO2 Protein, MTU1 Protein, TRMT Protein, TRMT1 Protein, TRNT1 Protein, 1110005N20Rik Protein, 1600025P05Rik Protein, AI314320 Protein, Trmt1 Protein, zgc:110555 Protein, tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase Protein, TRMU Protein, Trmu Protein, trmu Protein
    背景
    This nuclear gene encodes a mitochondrial tRNA-modifying enzyme. The encoded protein catalyzes the 2-thiolation of uridine on the wobble positions of tRNA(Lys), tRNA(Glu), and tRNA(Gln), resulting in the formation of 5-taurinomethyl-2-thiouridine moieties. Mutations in this gene may cause transient infantile liver failure. Polymorphisms in this gene may also influence the severity of deafness caused by mitochondrial 12S ribosomal RNA mutations. Alternative splicing results in multiple transcript variants.
    分子量
    47.6 kDa
    NCBI登录号
    NP_060476
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