DNA Repair Protein Complementing XP-G Cells (ERCC5) Peptide
ERCC5
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all ERCC5 products
- ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-ERCC5 antibody (Catalog #: ARP54287_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
- 别名
- COFS3 Peptide, ERCM2 Peptide, UVDR Peptide, XPG Peptide, XPGC Peptide, cofs3 Peptide, ercm2 Peptide, uvdr Peptide, xpg Peptide, xpgc Peptide, Xpg Peptide, ERCC excision repair 5, endonuclease Peptide, excision repair cross-complementation group 5 L homeolog Peptide, excision repair cross-complementing rodent repair deficiency, complementation group 5 Peptide, ERCC5 Peptide, ercc5.L Peptide, Ercc5 Peptide
- 背景
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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.
Alias Symbols: COFS3, ERCM2, UVDR, XPG, XPGC
Protein Interaction Partner: ERCC2,ERCC6,EWSR1,GTF2H1,GTF2H4,NTHL1,PCNA,POLR2A,CDK7,ERCC2,ERCC3,NTHL1,PCNA,TAF10
Protein Size: 1186 - 分子量
- 133 kDa
- 基因ID
- 2073
- NCBI登录号
- NM_000123, NP_000114
- UniProt
- P28715
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