Restriction Enzymes Cloning
Description
Restriction enzyme cloning is a fundamental technique for generating recombinant DNA. The process begins with a gene of interest and a bacterial plasmid, both digested using the same restriction enzyme, generating compatible ends. The gene and plasmid fragments are joined together through ligation, creating a transformed plasmid. The recombinant plasmid is then introduced into a host organism like bacteria for replication, enabling further study, protein expression, or other downstream applications. This molecular biology technique has numerous research and biotechnological applications. [Adapted from GPT4, 2023]
Acknowledgements
References
https://www.addgene.org/protocols/subcloning/
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