Faster and cheaper PCR on a standard thermocycler.
Author(s) -
Krzysztof Sobczak,
Piotr Kozłowski,
Włodzimierz J. Krzyżosiak
Publication year - 1995
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.1995_4635
Subject(s) - chemistry , denaturation (fissile materials) , polymerase chain reaction , dna , volume (thermodynamics) , computational biology , computer science , microbiology and biotechnology , chromatography , biology , biochemistry , physics , gene , thermodynamics , nuclear chemistry
The PCR conditions have been optimized to make the process faster and more economical. When short DNA fragments are to be amplified, the time of denaturation, annealing and extension steps can be as short as 1 s each, and the yield of PCR product is still high, sufficient for many types of analysis. The PCR can be done even in a reaction volume as low as 1 microliter. The recommended volume, 2.5 microliters or 5 microliters, allows significant savings in the laboratory budget especially for laboratories which use PCR frequently and on a large scale.
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