Genotyping the Deletion and Analyzing qPCR Results
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Analysis of CRISPR/Cas9 Mediated Deletion in F1 ES Cells
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Conclusion
副本
The overall goal of this procedure is to use allele specific CRISPR/Cas9 mediated deletion to study regulation of gene transcription in mouse embryonic stem cells. The main advantage of this technique, which uses a hybrid genome to generate and an
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Experimental validation of enhancer activity is best approached by loss-of-function analysis. Presented here is an efficient protocol that uses CRISPR/Cas9 mediated deletion to study allele-specific regulation of gene transcription in F1 ES cells which contain a hybrid genome (Mus musculus129 x Mus castaneus).