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  2. Polymerase chain reaction optimization - Wikipedia

    en.wikipedia.org/wiki/Polymerase_chain_reaction...

    Annealing of the 3' end of one primer to itself or the second primer may cause primer extension, resulting in the formation of so-called primer dimers, visible as low-molecular-weight bands on PCR gels. [15] Primer dimer formation often competes with formation of the DNA fragment of interest, and may be avoided using primers that are designed ...

  3. Asymmetric PCR - Wikipedia

    en.wikipedia.org/wiki/Asymmetric_PCR

    Asymmetric PCR is a variation of PCR used to preferentially amplify one strand of the original DNA more than the other. [1] The technique has applications in some types of sequencing and hybridization probing where having only one of the two complementary strands is required.

  4. In silico PCR - Wikipedia

    en.wikipedia.org/wiki/In_silico_PCR

    The last 10-12 bases at the 3' end of a primer are sensitive to initiation of polymerase extension and general primer stability on the template binding site. The effect of a single mismatch at these last 10 bases at the 3' end of the primer depends on its position and local structure, reducing the primer binding, selectivity, and PCR efficiency ...

  5. Polymerase chain reaction - Wikipedia

    en.wikipedia.org/wiki/Polymerase_chain_reaction

    A strip of eight PCR tubes, each containing a 100 μL reaction mixture Placing a strip of eight PCR tubes into a thermal cycler. 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.

  6. Hot start PCR - Wikipedia

    en.wikipedia.org/wiki/Hot_start_PCR

    Similarly, primer dimers form complexes which decreases the amount of copy number amplifications obtained. [10] This can be controlled by implementing hot start PCR which allows primer extensions to be blocked until the optimal temperatures are met. [2]

  7. Reverse transcription polymerase chain reaction - Wikipedia

    en.wikipedia.org/wiki/Reverse_transcription...

    RT-PCR. Reverse transcription polymerase chain reaction (RT-PCR) is a laboratory technique combining reverse transcription of RNA into DNA (in this context called complementary DNA or cDNA) and amplification of specific DNA targets using polymerase chain reaction (PCR). [1] It is primarily used to measure the amount of a specific RNA.

  8. Taq polymerase - Wikipedia

    en.wikipedia.org/wiki/Taq_polymerase

    It is frequently used in the polymerase chain reaction (PCR), a method for greatly amplifying the quantity of short segments of DNA. T. aquaticus is a bacterium that lives in hot springs and hydrothermal vents, and Taq polymerase was identified [1] as an enzyme able to withstand the protein-denaturing conditions (high temperature) required ...

  9. Primer dimer - Wikipedia

    en.wikipedia.org/wiki/Primer_dimer

    A primer dimer (PD) is a potential by-product in the polymerase chain reaction (PCR), a common biotechnological method. As its name implies, a PD consists of two primer molecules that have attached ( hybridized ) to each other because of strings of complementary bases in the primers.

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