XPA 抗体 (AA 1-273)
Quick Overview for XPA 抗体 (AA 1-273) (ABIN5775933)
抗原
See all XPA 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 1-273
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免疫原
- Recombinant human XPA (1-273aa) purified from E. coli
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亚型
- IgG1 kappa
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anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (Center) antibody
XPA 适用: 人 WB, IF, IHC (p), IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 1-273) antibodyXPA 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 2E4 unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 1-273) antibodyXPA 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 1-273) antibodyXPA 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (Internal Region) antibodyXPA 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 211-260) antibodyXPA 适用: 人, 小鼠 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 221-250), (C-Term) antibodyXPA 适用: 人 WB, IHC (p), FACS 宿主: 兔 Polyclonal RB23644 unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (AA 185-213), (C-Term) antibodyXPA 适用: 人 WB 宿主: 兔 Polyclonal RB33699 unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (C-Term) antibodyXPA 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Xeroderma Pigmentosum, Complementation Group A (XPA) (C-Term) antibodyXPA 适用: 人, 小鼠, 大鼠, 犬, Cow, 猴, Pig, Bat WB 宿主: 兔 Polyclonal unconjugated
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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储存条件
- 4 °C,-20 °C,-80 °C
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储存方法
- Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
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- XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))
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别名
- XPA
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背景
- XPA, also known as DNA repair protein complementing XP-A cells, belong to the XPA family. This protein is involved in DNA excision repair. It Initiates repair by binding to damaged sites with various affinities, depending on the photoproduct and the transcriptional state of the region. Defects in XPA are a cause of xeroderma pigmentosum complementation group A (XP-A), which is a rare human autosomal recessive disease characterized by solar sensitivity, high predisposition for developing cancers on areas exposed to sunlight and, in some cases, neurological abnormalities.
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NCBI登录号
- NP_000371
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途径
- DNA Damage Repair
抗原
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