Method for closing target gene and removing HBV e antigen based on base editing technology
A base editing and target gene technology, applied in genetic engineering, recombinant DNA technology, biochemical equipment and methods, etc., can solve problems such as HBV cannot be completely cured, viral DNA double-strand breaks, etc., and achieve high editing efficiency and precision, The effect of less dependence and strong security
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[0028] The invention will be further described below in combination with specific embodiments.
[0029] Such as Figure 1-3 As shown, a method based on base editing technology to close the target gene to clear HBV e antigen, analyze the positive strand of the HBV genome contained in HepG2.215 and HepAD38, determine the target of base editing, design and synthesize ABE8e and BE4 -max paired universal sgRNA primers targeting the edited inactive PreC ATG codon, connected to the pGL3-U6-sgRNA-PGK-EGFP or pGL3-U6sgRNA-accg-puro vector recovered after digestion with BsaI, transformed into Escherichia coli DH5α, Pick positive colonies and clones, and extract the plasmids in a small way. After the enzyme digestion and sequencing are identified correctly, the plasmids are extracted in large quantities for later use.
[0030] The method for constructing a carrier comprises the steps:
[0031] a: Prepare sgRNA plasmid
[0032] (1) Using the default parameters of DNAstar, analyze the p...
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