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Comparison of the effects of introducing the CRISPR/Cas9 system by microinjection and electroporation into porcine embryos at different stages

机译:通过显微注射和电穿孔将CRISPR / CAS9系统引入不同阶段的猪胚胎效果的比较

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摘要

Introduction of the CRISPR/Cas9 system targeting the B4GALNT gene into embryos by electroporation. a Cleavage and b blastocyst formation rates of electroporated embryos. Five replicates were analyzed for each treatment group. c Genotype of blastocysts, determined using Sanger sequencing and TIDE analysis. The proportions were calculated by dividing the number of gene-edited (bi-allelic and mosaic) blastocysts by the total number of sequenced blastocysts. bi: blastocysts having bi-allelic mutations, mos: blastocysts having mosaic mutations. d Mutation efficiency of gene-edited blastocysts. The mean proportions represent the proportion of indel mutation events in gene-edited blastocysts. The numbers within parentheses under the X-axis indicate the total number of examined samples. Error bars indicate mean ± SEM (a, c). a−c, A−CBars with different letters differ significantly (P < 0.05)
机译:通过电穿孔将CRISPR / CAS9系统靶向B4Galnt基因的胚胎。电穿孔胚胎的切割和B胚泡形成率。针对每个治疗组分析五种重复。 C基因型的胚泡,使用Sanger测序和潮汐分析测定。通过将基因编辑(Bi-Bibelic和Mosaic)胚泡的总数除以测序的胚泡总数来计算比例。 BI:具有双等异位突变的胚泡,MOS:具有马赛克突变的胚泡。 D基因编辑胚泡的突变效率。平均比例代表基因编辑胚泡中的吲哚突变事件的比例。 X轴下括号内的数字表示检查样本的总数。误差条表示平均值±SEM(A,C)。 A-C,具有不同字母的A-CBAR显着差异(P <0.05)

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