Literature DB >> 8588490

Faster and cheaper PCR on a standard thermocycler.

K Sobczak1, P Kozłowski, W J Krzyzosiak.   

Abstract

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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Year:  1995        PMID: 8588490

Source DB:  PubMed          Journal:  Acta Biochim Pol        ISSN: 0001-527X            Impact factor:   2.149


  2 in total

1.  Combined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection.

Authors:  P Kozlowski; W J Krzyzosiak
Journal:  Nucleic Acids Res       Date:  2001-07-15       Impact factor: 16.971

2.  PCR-SSCP-HDX analysis of pooled DNA for more rapid detection of germline mutations in large genes. The BRCA1 example.

Authors:  P Kozłowski; K Sobczak; M Napierała; M Woźniak; J Czarny; J Włodzimierz; J Kryzosiak
Journal:  Nucleic Acids Res       Date:  1996-03-15       Impact factor: 16.971

  2 in total

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