ERCC2 抗体
Quick Overview for ERCC2 抗体 (ABIN7257960)
抗原
See all ERCC2 抗体适用
宿主
克隆类型
标记
应用范围
- 
    - 
                                            产品特性
- Polyclonal Antibody
- 
                                            纯化方法
- Affinity purification
- 
                                            免疫原
- Recombinant fusion protein of human ERCC2 (NP_001124339.1).
- 
                                            亚型
- IgG
 
- 
                                            
- 
    
- 
    - 
                                            应用备注
- WB 1:500-1:2000
- 
                                            限制
- 仅限研究用
 
- 
                                            
- 
    - 
                                            状态
- Liquid
- 
                                            浓度
- 1 mg/mL
- 
                                            缓冲液
- PBS with 0.02 % sodium azide, 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
- Store at -20°C. Avoid freeze / thaw cycles.
 
- 
                                            
- 
    - ERCC2 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 (ERCC2))
- 
                                            别名
- ERCC2
- 
                                            背景
- The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
- 
                                            分子量
- 
                        Observed_MW: 80 kDa Calculated_MW: 46 kDa/86 kDa 
- 
                                            基因ID
- 2068
- 
                                            UniProt
- P18074
- 
                                            途径
- DNA Damage Repair
 抗原
- 
                    
 
                                     
                                     
                                    