Skip to main content

Limitations and Troubleshooting

  • Chapter
Molecular Diagnostic PCR Handbook
  • 2330 Accesses

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 179.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 229.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 249.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

3. References

  1. Akane, C.E. 1994. Identification of the heme compound co-purified with deoxyribonucleic acid (DNA) from blood strains, a major inhibitor of PCR. J. of Forensic Science, 39, 362–372

    CAS  Google Scholar 

  2. Bell, D.A. 1991. Excessive cycling converts PCR products to random length higher molecular weight fragments. Nucl Acids Res, 19(18), 5079

    PubMed  CAS  Google Scholar 

  3. Chou, O. 1992. Prevention of pre-PCR mis-priming and primer dimerization improves low-copy-number amplifications. Nucl Acids Res, 20(7), 1717–1723

    PubMed  CAS  Google Scholar 

  4. Dieffenbach, C. 1993. Setting up a PCR laboratory. PCR Methods and Applications, 3, S2–S7

    PubMed  CAS  Google Scholar 

  5. Dragon, E. 1993. Handling Reagents in the PCR Laboratory. PCR Methods and Applications, 3, S8–S9

    PubMed  CAS  Google Scholar 

  6. Dohner, D. 1995. Inhibition of PCR by mineral oil exposed to UV irradiation for prolonged periods. BioTechniques, 18(6), 964–967

    PubMed  CAS  Google Scholar 

  7. Hanni, C. 1995. Isopropanol precipitation removes PCR inhibitors from ancient bone extracts. Nucl Acids Res, 23(5), 881–882

    PubMed  CAS  Google Scholar 

  8. Hartley, J. 1993. Dealing with Contamination: Enzymatic Control of Carryover Contamination in PCR. PCR Methods and Applications, 3(2), S10–S14

    PubMed  CAS  Google Scholar 

  9. Huang, S. 1994. Long-range jumping of incompletely extended polymerase chain fragments generates unexpected products. BioTechniques, 16(2), 242–246

    PubMed  CAS  Google Scholar 

  10. Lee, O.C. 1995. Improved direct PCR screen for bacterial colonies: wooden toothpicks inhibit PCR amplification. BioTechniques, 18(2), 225–226

    PubMed  CAS  Google Scholar 

  11. Longo, P. 1990. Use of uracil DNA glycosylase to control carry-over contamination in polymerase chain reactions. Gene, 9, 125–128

    Google Scholar 

  12. Menon, R. 1991. RT-PCR artifacts from processed pseudogenes. PCR Methods and Applications, 1, 70–71

    PubMed  CAS  Google Scholar 

  13. Prince, S.E. 1992. PCR: How to Kill Unwanted DNA. BioTechniques, 12, 358–360

    PubMed  CAS  Google Scholar 

  14. Odelberg, S.J., Weiss, R.B., Hata, A., et al. 1995. Template switching during DNA synthesis by Thermus aquaticus DNA polymerase I. Nucl Acids Res, 23, 2049–2057

    PubMed  CAS  Google Scholar 

Download references

Rights and permissions

Reprints and permissions

Copyright information

© 2005 IAEA

About this chapter

Cite this chapter

(2005). Limitations and Troubleshooting. In: Molecular Diagnostic PCR Handbook. Springer, Dordrecht. https://doi.org/10.1007/1-4020-3404-0_4

Download citation

Publish with us

Policies and ethics