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. 2015 Nov 3;1:15031. doi: 10.1038/celldisc.2015.31

Figure 3.

Figure 3

Generation of ICAHCI offspring by H19Δ1AG-haESCs. (a) Blastocysts generated by injection of H19Δ1AG-haESCs into oocytes. The H19Δ1AG-haESCs carried the Oct4-eGFP transgene. (b) Three SC pups from ICAHCI using H19Δ1AG-haESCs. (c) Adult SC mice derived from ICAHCI using H19Δ1AG-haESCs. (d) PCR analysis of H19 deletion in SC mice. (e) Adult H19Δ1SC-Black mouse and its progeny. (f) PCR analysis of H19 deletion in the progeny of H19Δ1SC-Black mice. The primer pairs P1–P2 and P3–P4 were used. (g) Adult H19Δ1SC-Agouti mouse and its progeny. (h) PCR analysis of the H19 deletion in the progeny of SC-Agouti mice. (i) Methylation analysis of imprinting in H19Δ1SC pups. C57BL/6 mice DNA was used as control. Open circles represent unmethylated CpG sites, whereas filled circles represent methylated CpG sites.