Technique / Molecular Biology / PCR / GC-rich PCR

(GC-rich PCR technique papers)
1: Hube F, Reverdiau P, Iochmann S, Gruel Y.
Improved PCR method for amplification of GC-rich DNA sequences.
Mol Biotechnol. 2005 Sep;31(1):81-4. Review.

2: Bachmann HS, Siffert W, Frey UH.
Successful amplification of extremely GC-rich promoter regions using a novel
'slowdown PCR' technique.
Pharmacogenetics. 2003 Dec;13(12):759-66.

3: Moreau A, Wang DS, Forget S, Duez C, Dusart J.
GC-rich template amplification by inverse PCR. DNA polymerase and solvent
effects.
Methods Mol Biol. 2002;192:75-80.

4: Le Cam L, Polanowska J, Fajas L, Fabbrizio E, Sardet C.
Improved LM-PCR procedure for in vivo footprinting analysis of GC-rich
promoters.
Biotechniques. 1999 May;26(5):840-3.

5: Henke W, Herdel K, Jung K, Schnorr D, Loening SA.
Betaine improves the PCR amplification of GC-rich DNA sequences.
Nucleic Acids Res. 1997 Oct 1;25(19):3957-8.

6: Moreau A, Duez C, Dusart J.
GC-rich template amplification by inverse PCR. DNA polymerase and solvent
effects.
Methods Mol Biol. 1997;67:47-53.

7: Turner SL, Jenkins FJ.
Use of deoxyinosine in PCR to improve amplification of GC-rich DNA.
Biotechniques. 1995 Jul;19(1):48-52.

8: Moreau A, Duez C, Dusart J.
Improvement of GC-rich template amplification by inverse PCR.
Biotechniques. 1994 Aug;17(2):232-4. Erratum in:
Biotechniques 1994 Oct;17(4):684.

9: Agarwal RK, Perl A.
PCR amplification of highly GC-rich DNA template after denaturation by NaOH.
Nucleic Acids Res. 1993 Nov 11;21(22):5283-4.

10: Sun Y, Hegamyer G, Colburn NH.
PCR-direct sequencing of a GC-rich region by inclusion of 10% DMSO: application
to mouse c-jun.
Biotechniques. 1993 Sep;15(3):372-4.

11: Sheffield VC, Beck JS, Stone EM, Myers RM.
A simple and efficient method for attachment of a 40-base pair, GC-rich
sequence to PCR-amplified DNA.
Biotechniques. 1992 Mar;12(3):386-8.