Targeted sequencing of Ripk1 mouse gene treated with AAV-SaCas9
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1090862
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资源简介：
To assess the role of RIPK1 in HDV-mediated liver injury, we developed a CRISPR/Cas9 gene editing system that specifically knockdown RIPK1 expression in hepatocytes. We achieve this by expressing the Cas9 protein under the control of a liver specific promoter that was delivered using a rAAV vector with hepatic tropism.
创建时间：
2024-03-22
