ERCC5 抗体 (C-Term)
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Quick Overview for ERCC5 抗体 (C-Term) (ABIN1536666)
抗原
See all ERCC5 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 1151-1178, C-Term
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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免疫原
- This ERCC5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1151-1178 amino acids from the C-terminal region of human ERCC5.
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亚型
- Ig Fraction
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anti-DNA Repair Protein Complementing XP-G Cells (ERCC5) (AA 778-986) antibody
ERCC5 适用: 人 WB, ELISA, IHC (p), ICC, IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-DNA Repair Protein Complementing XP-G Cells (ERCC5) (N-Term) antibodyERCC5 适用: 人 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-DNA Repair Protein Complementing XP-G Cells (ERCC5) (N-Term) antibodyERCC5 适用: 人, 猴 WB, IHC, IF, IC 宿主: 兔 Polyclonal unconjugated
anti-DNA Repair Protein Complementing XP-G Cells (ERCC5) (N-Term) antibodyERCC5 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-DNA Repair Protein Complementing XP-G Cells (ERCC5) (AA 1-1186) antibodyERCC5 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-DNA Repair Protein Complementing XP-G Cells (ERCC5) (AA 182-231) antibodyERCC5 适用: 人, 小鼠, 大鼠, 猴, Cow, 犬, 马, 兔 WB 宿主: 兔 Polyclonal unconjugated
anti-DNA Repair Protein Complementing XP-G Cells (ERCC5) (N-Term) antibodyERCC5 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:1000
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- ERCC5 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
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有效期
- 6 months
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- ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
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别名
- ERCC5
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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. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined. [provided by RefSeq].
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分子量
- 133108
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基因ID
- 2073
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NCBI登录号
- NP_000114
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UniProt
- P28715
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途径
- DNA Damage Repair
抗原
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