通过CRISPR/Cas9技术,设计并实现了包含1559bp的缺失,包括1号外显子,使用了sgRNAs针对靶序列TCCCTGAACCAGCCCCCCAA和GGGTTGGGCCGGCTCCCAGA。RNA测序和 Western blot结果显示,这个等位基因没有表达。(来源:J:302139)
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A 559 bp deletion including exon 1 was engineered using sgRNAs (targeting TCCCTGAACCAGCCCCCCAA and GGGTTGGGCCGGCTCCCAGA) with CRISPR/Cas9 technology. RNA sequencing and Western blot analysis confirmed lack of expression from this allele. (J:302139)