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  1. La reacción en cadena de la polimerasa, o PCR, es una técnica para hacer muchas copias de una determinada región de ADN in vitro (en un tubo de ensayo en lugar de un organismo). La PCR depende de una ADN polimerasa termoestable, la Taq polimerasa , y requiere de cebadores de ADN diseñados específicamente para la región de ADN de interés.

  2. Polymerase chain reaction, or PCR, is a technique to make many copies of a specific DNA region in vitro (in a test tube rather than an organism). PCR relies on a thermostable DNA polymerase, Taq polymerase , and requires DNA primers designed specifically for the DNA region of interest.

  3. 6 de mar. de 2023 · The polymerase chain reaction (PCR) is a laboratory nucleic acid amplification technique used to denature and renature short segments of deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) sequences using DNA polymerase I enzyme, an isolate from Thermus aquaticus, known as Taq DNA.

  4. The polymerase chain reaction (PCR) is a method widely used to make millions to billions of copies of a specific DNA sample rapidly, allowing scientists to amplify a very small sample of DNA (or a part of it) sufficiently to enable detailed study.

  5. 17 de may. de 2024 · polymerase chain reaction ( PCR), a technique used to make numerous copies of a specific segment of DNA quickly and accurately. The polymerase chain reaction enables investigators to obtain the large quantities of DNA that are required for various experiments and procedures in molecular biology , forensic analysis , evolutionary biology , and ...

  6. 17 de may. de 2024 · PCR, o la reacción en cadena de la polimerasa, es una reacción química que los biólogos moleculares utilizan para amplificar (crear copias) fragmentos de ADN. Esta reacción permite que unos pocos fragmentos de ADN se repliquen en millones o miles de millones de copias.

  7. 9 de nov. de 2017 · PCR (Polymerase Chain Reaction) is a revolutionary method developed by Kary Mullis in the 1980s. PCR is based on using the ability of DNA polymerase to synthesize new strand of DNA complementary to the offered template strand. Because DNA polymerase can add a nucleotide only onto a preexisting 3'-OH group, it needs a primer to which ...

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