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The chapter discusses critical tools and techniques in genetic engineering, focusing on how enzymes and processes manipulate DNA. It covers the functions of restriction enzymes and ligases, the Polymerase Chain Reaction (PCR) used for DNA amplification, and gel electrophoresis, which separates DNA fragments by size. These fundamental concepts provide a foundational understanding of modern genetic engineering practices.
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Term: Restriction Enzymes
Definition: Enzymes that cut DNA at specific sequences, used in cloning and recombinant DNA technology.
Term: DNA Ligase
Definition: An enzyme that joins DNA fragments by forming covalent bonds, crucial for gene editing.
Term: Polymerase Chain Reaction (PCR)
Definition: A technique that amplifies specific DNA segments, producing millions of copies for various applications.
Term: Gel Electrophoresis
Definition: A method for separating DNA fragments by size through an electric field, allowing for visualization and analysis.
Term: Plasmids
Definition: Circular DNA molecules used as vectors for carrying foreign genes within a host organism.
Term: Taq Polymerase
Definition: A heat-resistant enzyme used in PCR to synthesize new DNA strands.
Term: Primers
Definition: Short DNA sequences that initiate the DNA synthesis process during PCR.
Term: Microinjection
Definition: A technique to inject DNA directly into cells, allowing for genetic modification.