CRISPR/Cas9基因编辑被用来去除基因的5'UTR和起始外显子,具体是310bp的c.249_61del区域。通过RT-PCR和 Western blot检测,确认了mRNA和蛋白质均未表达(来源:J:243374)。
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CRISPR/Cas9 gene editing was used to delete a portion of the 5'UTR and the first exon of the gene (310 bp c.249_61del). RT-PCR and Western blot analysis confirmed absence of mRNA and protein. (J:243374)