ExtFig3A_RACE_BCAP31_R3_LG293_annotated.tiff
收藏DataCite Commons2023-01-19 更新2024-08-18 收录
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https://figshare.com/articles/dataset/ExtFig3A_RACE_BCAP31_R3_LG293_annotated_tiff/21804513/1
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<em>Xrn1 knock out A549 cells were infected with WT PR8 or PR8-PA(∆X), or mock infected. 5’ RACE was then performed using primers specific for BCAP31, TUBA1B, INSIG1 or SLC7A5, positioned ~ 200-300 nucleotides downstream of the predicted cut sites.The PCR products were run on an agarose gel. </em>
将Xrn1基因敲除的A549细胞分别用野生型(WT)PR8毒株、PR8-PA(∆X)毒株感染,另设空白感染对照组。随后以针对BCAP31、TUBA1B、INSIG1及SLC7A5的特异性引物开展5' 末端快速扩增(5' RACE)实验,引物位点均位于各靶基因预测剪切位点下游约200~300个核苷酸区域。将所得聚合酶链式反应(Polymerase Chain Reaction, PCR)产物进行琼脂糖凝胶电泳。
提供机构:
figshare
创建时间:
2023-01-19



