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The volume needed can then be calculated as follows: 1.25 Units x (1 µl / 5 Units) = 0.25 µl. The template DNA volume required depends on your sample type. You should add about 1 pg to 10 ng of plasmid or viral DNA, and 1 ng to 1 µg of genomic DNA.
Polymerase chain reaction, or PCR, is a laboratory technique used to make multiple copies of a segment of DNA. PCR is very precise and can be used to amplify, or copy, a specific DNA target from a mixture of DNA molecules.
Polymerase chain reaction (abbreviated PCR) is a laboratory technique for rapidly producing (amplifying) millions to billions of copies of a specific segment of DNA, which can then be studied in greater detail.
Like DNA replication in an organism, PCR requires a DNA polymerase enzyme that makes new strands of DNA, using existing strands as templates. The DNA polymerase typically used in PCR is called Taq polymerase, after the heat-tolerant bacterium from which it was isolated (Thermus aquaticus).
5 basic components are required for the PCR process. These are: DNA template, DNA polymerase enzyme (or Taq polymerase enzyme), primers, nucleotides, and reaction buffers.