Using an sgRNA and CRISPR/Cas9 technology, a FLAG sequence was inserted at the 3' end of the coding sequence immediately upstream of the stop codon. The sgRNA- and Cas9-expressing plasmid and reference plasmid were transfected into EGR-G01 ES cells. The ES cells were then injected into 8-cell ICR embryos. (J:243766)
Basic Information
(129S2/SvPas x C57BL/6NSlc)F1-Tg(CAG-EGFP,Acr-EGFP)2Osb
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count