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ERCC3 抗体

ERCC3 适用: 人, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7113553
发货至: 中国
  • 抗原 See all ERCC3 抗体
    ERCC3 (DNA Repair Protein Complementing XP-B Cells (ERCC3))
    适用
    • 46
    • 29
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    • 3
    • 1
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    人, 小鼠
    宿主
    • 37
    • 8
    • 1
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    克隆类型
    • 40
    • 7
    多克隆
    标记
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    This ERCC3 antibody is un-conjugated
    应用范围
    • 36
    • 13
    • 13
    • 10
    • 7
    • 7
    • 6
    • 4
    • 3
    • 2
    • 1
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    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    纯化方法
    Immunogen affinity purified
    纯度
    ≥95 % as determined by SDS-PAGE
    免疫原
    excision repair cross-complementing rodent repair deficiency, complementation group 3 (xeroderma pigmentosum group B complementing)
    亚型
    IgG
    Top Product
    Discover our top product ERCC3 Primary Antibody
  • 应用备注
    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide and 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
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    有效期
    12 months
  • 抗原
    ERCC3 (DNA Repair Protein Complementing XP-B Cells (ERCC3))
    别名
    ERCC3 (ERCC3 产品)
    别名
    BTF2 antibody, GTF2H antibody, RAD25 antibody, TFIIH antibody, XPB antibody, BTF2 p89 antibody, Ercc-3 antibody, wu:fc25f08 antibody, ERCC excision repair 3, TFIIH core complex helicase subunit antibody, excision repair cross-complementing rodent repair deficiency, complementation group 3 antibody, excision repair cross-complementation group 3 antibody, ERCC3 antibody, Ercc3 antibody, ercc3 antibody
    背景
    Synonyms:XPB, XPBC Background:This gene encodes an ATP-dependent DNA helicase that functions in nucleotide excision repair. The encoded protein is a subunit of basal transcription factor 2 (TFIIH) and, therefore, also functions in class II transcription. Mutations in this gene are associated with Xeroderma pigmentosum B, Cockayne's syndrome, and trichothiodystrophy. Alternative splicing results in multiple transcript variants.
    分子量
    80 kDa
    基因ID
    2071
    UniProt
    P19447
    途径
    DNA Damage Repair
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