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RNASEH2A Protein (Myc-DYKDDDDK Tag)

RNASEH2A 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 ABIN2730998
发货至: 中国
  • 抗原 See all RNASEH2A 蛋白
    RNASEH2A (Ribonuclease H2, Subunit A (RNASEH2A))
    蛋白类型
    Recombinant
    宿主
    • 3
    • 2
    • 1
    • 1
    资源
    • 3
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This RNASEH2A protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human RNASEH2A 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 RNASEH2A 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
    RNASEH2A (Ribonuclease H2, Subunit A (RNASEH2A))
    别名
    Rnaseh2a (RNASEH2A 产品)
    别名
    2400006P09Rik Protein, RNASEHI Protein, RNHIA Protein, RNHL Protein, zgc:56307 Protein, AGS4 Protein, JUNB Protein, ribonuclease H2 subunit A Protein, ribonuclease H2, large subunit Protein, ribonuclease H2, subunit A Protein, ribonuclease H2 subunit A L homeolog Protein, rnaseh2a Protein, RNASEH2A Protein, Rnaseh2a Protein, rnaseh2a.L Protein
    背景
    The protein encoded by this gene is a component of the heterotrimeric type II ribonuclease H enzyme (RNAseH2). RNAseH2 is the major source of ribonuclease H activity in mammalian cells and endonucleolytically cleaves ribonucleotides. It is predicted to remove Okazaki fragment RNA primers during lagging strand DNA synthesis and to excise single ribonucleotides from DNA-DNA duplexes. Mutations in this gene cause Aicardi-Goutieres Syndrome (AGS), a an autosomal recessive neurological disorder characterized by progressive microcephaly and psychomotor retardation, intracranial calcifications, elevated levels of interferon-alpha and white blood cells in the cerebrospinal fluid.[provided by RefSeq, Aug 2009].
    分子量
    33.2 kDa
    NCBI登录号
    NP_006388
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