B组着色性干皮病偶联因子(XPB)活性蛋白
Active Xeroderma Pigmentosum, Complementation Group B (XPB)
ERCC3; XPBC; BTF2; RAD25; TFIIH; GTF2H; Excision Repair Cross-Complementing Rodent Repair Deficiency,Complementation Group 3; Basic transcription factor 2 89 kDa subunit
活性实验
Xeroderma Pigmentosum, Complementation Group B (XPB) is a crucial DNA helicase encoded by the ERCC3 gene in humans. As a component of the transcription factor IIH (TFIIH) complex, XPB plays dual roles in nucleotide excision repair (NER) and transcription initiation. In NER, it unwinds DNA around lesion sites to facilitate damage removal, while in transcription, it helps open promoter regions for RNA polymerase II. Besides,Poly U Binding Splicing Factor 60kDa (PUF60) has been identified as an interactor of XPB, thus a functional binding ELISA assay was conducted to detect the interaction of recombinant human XPB and recombinant human PUF60 .Briefly, biotin-linked XPB were diluted serially in PBS, with 0.01% BSA (pH 7.4). Duplicate samples of 100μl were then transferred to PUF60-coated microtiter wells and incubated for 1h at 37℃. Wells were washed with PBST 3 times and incubation with Streptavidin-HRP for 30min, then wells were aspirated and washed 5 times. With the addition of substrate solution, wells were incubated 15-25 minutes at 37℃. Finally, add 50µl stop solution to the wells and read at 450nm immediately. The binding activity of recombinant human XPB and recombinant human PUF60 was shown in Figure 1, the EC50 for this effect is 0.29 µg/mL.
用法
Reconstitute in 10mM PBS (pH7.4) to a concentration of 0.1-1.0 mg/mL. Do not vortex.
储存
避免反复冻融。2-8°C不超过一个月,-80°C不超过12个月。
稳定性
热稳定性以损失率显示。损失率是由加速降解试验决定,具体方法如下:在37°C孵育48小时,没有显著的降解或者沉淀产生。保质期内,在适当的条件下存储,损失率低于5%。
增值服务
相关产品
| 编号 | 适用物种:Homo sapiens (Human,人) | 应用(仅供研究使用,不用于临床诊断!) |
| APE732Hu01 | B组着色性干皮病偶联因子(XPB)活性蛋白 | Cell culture; Activity Assays. |
| RPE732Hu01 | B组着色性干皮病偶联因子(XPB)重组蛋白 | Positive Control; Immunogen; SDS-PAGE; WB. |



