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Respondido por UpStudy AI y revisado por un tutor profesional
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Bonus Knowledge
The process of amplifying DNA often begins with a tiny sample, like a single cell or a drop of blood. This technique, known as polymerase chain reaction (PCR), uses temperature changes to denature the DNA, allowing specific regions to be replicated millions of times. This incredible sensitivity makes PCR invaluable in fields ranging from criminal forensics to medical diagnostics, enabling scientists to detect even the faintest traces of genetic material. To get the best results when amplifying DNA, it’s crucial to avoid cross-contamination. One common mistake is using the same pipette tips for multiple samples, which can introduce unwanted DNA. Another tip is to ensure that your reagents are fresh and properly stored; degraded polymerases can significantly impact the efficiency of your amplification and lead to unexpected results. Preventing these pitfalls will help make your DNA amplification projects successful and exciting!
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