电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

RNASEH2A 抗体

RNASEH2A 适用: 人, 大鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6568584
发货至: 中国
  • 抗原 See all RNASEH2A 抗体
    RNASEH2A (Ribonuclease H2, Subunit A (RNASEH2A))
    适用
    • 21
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 大鼠
    宿主
    • 19
    • 4
    克隆类型
    • 22
    • 1
    多克隆
    标记
    • 20
    • 1
    • 1
    • 1
    This RNASEH2A antibody is un-conjugated
    应用范围
    • 19
    • 10
    • 10
    • 6
    • 5
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human RNASEH2A (NP_006388.2).
    亚型
    IgG
    Top Product
    Discover our top product RNASEH2A Primary Antibody
  • 应用备注
    WB 1:500-1:2000 IF 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    RNASEH2A (Ribonuclease H2, Subunit A (RNASEH2A))
    别名
    RNASEH2A (RNASEH2A 产品)
    别名
    2400006P09Rik antibody, RNASEHI antibody, RNHIA antibody, RNHL antibody, zgc:56307 antibody, AGS4 antibody, JUNB antibody, ribonuclease H2 subunit A antibody, ribonuclease H2, large subunit antibody, ribonuclease H2, subunit A antibody, ribonuclease H2 subunit A L homeolog antibody, rnaseh2a antibody, RNASEH2A antibody, Rnaseh2a antibody, rnaseh2a.L antibody
    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.
    分子量

    Observed_MW: 33kDa

    Calculated_MW: 33kDa

    基因ID
    10535
    UniProt
    O75792
You are here:
客服