Literature DB >> 7859166

RAPD reactions from crude plant DNA. Adding RNase A as a "helper enzyme".

B Heinze1.   

Abstract

As opposed to standard polymerase chain reaction (PCR) using specific primers, genome analysis involving short random primers, for example RAPD, may yield inconsistent results if crude plant DNA preparations are used as the template. When RNase A, a thermostable enzyme, was added to such reactions, highly repeatable banding patterns were obtained from crude plant DNA, thus speeding up analyses substantially.

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Year:  1994        PMID: 7859166     DOI: 10.1007/bf02921697

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  10 in total

1.  DNA amplification fingerprinting using very short arbitrary oligonucleotide primers.

Authors:  G Caetano-Anollés; B J Bassam; P M Gresshoff
Journal:  Biotechnology (N Y)       Date:  1991-06

2.  A simple and rapid method for the preparation of plant genomic DNA for PCR analysis.

Authors:  K Edwards; C Johnstone; C Thompson
Journal:  Nucleic Acids Res       Date:  1991-03-25       Impact factor: 16.971

3.  DNA polymorphisms amplified by arbitrary primers are useful as genetic markers.

Authors:  J G Williams; A R Kubelik; K J Livak; J A Rafalski; S V Tingey
Journal:  Nucleic Acids Res       Date:  1990-11-25       Impact factor: 16.971

4.  Reverse transcription of mRNA by Thermus aquaticus DNA polymerase followed by polymerase chain reaction amplification.

Authors:  M D Jones
Journal:  Methods Enzymol       Date:  1993       Impact factor: 1.600

5.  Suppression of PCR amplification by high levels of RNA.

Authors:  M J Pikaart; B Villeponteau
Journal:  Biotechniques       Date:  1993-01       Impact factor: 1.993

6.  Concentration of primer and template qualitatively affects products in random-amplified polymorphic DNA PCR.

Authors:  K Muralidharan; E K Wakeland
Journal:  Biotechniques       Date:  1993-03       Impact factor: 1.993

7.  Artifactual variation in randomly amplified polymorphic DNA banding patterns.

Authors:  D L Ellsworth; K D Rittenhouse; R L Honeycutt
Journal:  Biotechniques       Date:  1993-02       Impact factor: 1.993

8.  Pretreatment with RNase to improve PCR amplification of DNA using 10-mer primers.

Authors:  C S Yoon; D A Glawe
Journal:  Biotechniques       Date:  1993-06       Impact factor: 1.993

9.  Fingerprinting genomes using PCR with arbitrary primers.

Authors:  J Welsh; M McClelland
Journal:  Nucleic Acids Res       Date:  1990-12-25       Impact factor: 16.971

10.  Use of PCR primers containing a 3'-terminal ribose residue to prevent cross-contamination of amplified sequences.

Authors:  R Y Walder; J R Hayes; J A Walder
Journal:  Nucleic Acids Res       Date:  1993-09-11       Impact factor: 16.971

  10 in total

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