CRISPR/Cas9 technology was used to target the entire open reading frame and create a deletion of 2,324 bp in exon 2. Quantitative RT-PCR analysis confirmed the complete absence of mRNA expression in the testes of homozygous mutant mice. (J:324150)
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CRISPR/Cas9 technology was used to target the entire open reading frame and create a deletion of 2,324 bp in exon 2. Quantitative RT-PCR analysis confirmed the complete absence of mRNA expression in the testes of homozygous mutant mice. (J:324150)