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ERCC5 抗体

ERCC5 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2459724
发货至: 中国
  • 抗原 See all ERCC5 抗体
    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
    适用
    • 44
    • 11
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    • 1
    人, 小鼠, 大鼠
    宿主
    • 40
    • 4
    克隆类型
    • 41
    • 3
    多克隆
    标记
    • 27
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
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    This ERCC5 antibody is un-conjugated
    应用范围
    • 33
    • 18
    • 8
    • 6
    • 5
    • 4
    • 3
    • 1
    • 1
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    • 1
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    Western Blotting (WB), ELISA
    纯化方法
    Antibody is purified by peptide affinity chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ERCC5.
    Top Product
    Discover our top product ERCC5 Primary Antibody
  • 应用备注
    ERCC5 antibody can be used for detection of ERCC5 by ELISA at 1:62500. ERCC5 antibody can be used for detection of ERCC5 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    浓度
    1 mg/mL
    缓冲液
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    注意事项
    As with any antibody avoid repeat freeze-thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store ERCC5 antibody at -20 °C.
  • 抗原
    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
    别名
    ERCC5 (ERCC5 产品)
    别名
    COFS3 antibody, ERCM2 antibody, UVDR antibody, XPG antibody, XPGC antibody, cofs3 antibody, ercm2 antibody, uvdr antibody, xpg antibody, xpgc antibody, Xpg antibody, ERCC excision repair 5, endonuclease antibody, excision repair cross-complementation group 5 L homeolog antibody, excision repair cross-complementing rodent repair deficiency, complementation group 5 antibody, ERCC5 antibody, ercc5.L antibody, Ercc5 antibody
    背景
    Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
    分子量
    133 kDa
    基因ID
    2073
    NCBI登录号
    NP_000114
    UniProt
    P28715
    途径
    DNA Damage Repair
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