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CRISPR-Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats-Cas9) is a revolutionary gene editing tool that has taken the field of molecular biology by storm. It allows scientists to precisely modify an organism's DNA at a specific location, offering unprecedented potential for research and therapeutic applications.
Imagine researchers studying a genetic disease caused by a single point mutation in a specific gene. They can design a CRISPR-Cas9 system where the guide RNA targets the mutated sequence. The Cas9 enzyme then creates a break in the DNA. The cell's natural repair machinery can be harnessed to insert a corrected DNA copy at the targeted location, effectively fixing the mutation and potentially curing the disease.
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