Literature DB >> 8457343

Two-step "hot" PCR amplification of GC-rich avian c-myc sequences.

M Schuchard1, G Sarkar, T Ruesink, T C Spelsberg.   

Abstract

A new two-step cycle PCR method has been developed for amplification of GC-rich DNA sequences. Using this method, termed "hot PCR," 111 and 179 bp regions (GC contents of 74% and 76%, respectively) of the avian c-myc proto-oncogene were specifically amplified from cloned and genomic DNA. This method uses high-melting primers (Tm between 70 degrees and 74 degrees C), a two-step cycle that employs a 94 degrees C denaturation step and an annealing-elongation step between 70 degrees and 80 degrees C with or without formamide.

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Year:  1993        PMID: 8457343

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  2 in total

1.  High temperature cDNA synthesis by AMV reverse transcriptase improves the specificity of PCR.

Authors:  B Fuchs; K Zhang; M G Rock; M E Bolander; G Sarkar
Journal:  Mol Biotechnol       Date:  1999-10       Impact factor: 2.695

2.  Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol.

Authors:  Zeinab Mousavian; Hamid Mir Mohammad Sadeghi; Ali Mohammad Sabzghabaee; Fatemeh Moazen
Journal:  Adv Biomed Res       Date:  2014-01-27
  2 in total

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