New FRET primers for quantitative real-time PCR
Artikel i vetenskaplig tidskrift, 2007

FRET primer real-time PCR chemistry depends on internally labeled primers with FRET dyes linked to their 3' end. The best distance between the FRET dyes for obtaining the largest signal and the lowest background is six nucleotides. In this study the forward primer was labeled with FAM and the reverse primer with Texas red; the labeled primers meet in cycle two of PCR. At the end of the elongation step FAM is excited to emit fluorescence which will excite Texas red to emit new fluorescence that correlates directly with the quantity of PCR product accumulated. FRET primer techniques amplify short amplicons with unique thermal cycling steps, 0 s at 85 degrees C for denaturation, 7 s for annealing, and 2 s for elongation. The FRET primer technique was very efficient (92.6, 97.2, and 100%), correlation coefficients were high (1.0, 0.999, and 0.999), and total run time was very short (20, 45, and 40 min per 40 cycles with LightCycler, iCycler, and RotorGene 3000, respectively). When FRET-labeled primers were compared with similar but unlabeled primers it was observed that the FRET primer technique had a lower Ct value and was more efficient than use of unlabeled primers detected by use of SYBR Green I.

ENERGY-TRANSFER

FRET Primers

quantitative real-time

Texas red

FAM

PCR

AMPLIFICATION

real-time PCR

DNA PROBES

labeled primers

POLYMERASE

HYBRIDIZATION

PRODUCT

Författare

Ashraf Ahmad

Chalmers, Kemi- och bioteknik

J. B. Ghasemi

Razi University

Analytical and Bioanalytical Chemistry

1618-2642 (ISSN) 1618-2650 (eISSN)

Vol. 387 2737-2743

Ämneskategorier

Kemiteknik

DOI

10.1007/s00216-007-1123-4