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DCLRE1B 抗体

DCLRE1B 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7262739
发货至: 中国
  • 抗原 See all DCLRE1B 抗体
    DCLRE1B (DNA Cross-Link Repair 1B (DCLRE1B))
    适用
    • 27
    • 8
    • 1
    人, 小鼠
    宿主
    • 26
    • 1
    克隆类型
    • 26
    • 1
    多克隆
    标记
    • 8
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DCLRE1B antibody is un-conjugated
    应用范围
    • 17
    • 17
    • 13
    • 2
    • 1
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human DCLRE1B (NP_073747.1).
    亚型
    IgG
    Top Product
    Discover our top product DCLRE1B Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    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
    DCLRE1B (DNA Cross-Link Repair 1B (DCLRE1B))
    别名
    DCLRE1B (DCLRE1B 产品)
    别名
    APOLLO antibody, SNM1B antibody, SNMIB antibody, im:6894074 antibody, zgc:154089 antibody, AI452214 antibody, Apollo antibody, mSNM1B antibody, DNA cross-link repair 1B antibody, DCLRE1B antibody, Dclre1b antibody, dclre1b antibody
    背景
    DCLRE1B (DNA Cross-Link Repair 1B) is a Protein Coding gene. Diseases associated with DCLRE1B include Hoyeraal Hreidarsson Syndrome and Dyskeratosis Congenita. Among its related pathways are Fanconi anemia pathway and DNA Double-Strand Break Repair. Gene Ontology (GO) annotations related to this gene include 5'-3' exonuclease activity. An important paralog of this gene is DCLRE1C.
    分子量

    Observed_MW: 60 kDa

    Calculated_MW: 60 kDa

    基因ID
    64858
    UniProt
    Q9H816
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