Skip to main content
Log in

DNA Extraction from small blood volumes and the processing of cellulose blood cards for use in polymerase chain reaction

  • Research
  • Published:
Molecular Biotechnology Aims and scope Submit manuscript

Abstract

This article describes two procedures for the purification of genomic DNA from small blood volumes of whole blood using DNAzol®BD. In the first procedure, DNA is isolated from 1–20 μL of whole blood using a fast and simple protocol that is appropriate for the simultaneous extraction of a large number of samples. The isolated DNA is suitable for gel electrophoresis and polymerase chain reaction (PCR). In the second procedure, cellulose blood cards containing approx 5 μL of dried blood are treated with DNAzol BD in order to retain DNA on the cellulose matrix while removing other cellular components. The blood card with DNA subsequently serves as template in PCR. The blood card processing and amplification procedures are performed in the same PCR tube without any centrifugation steps, making the combined procedures amenable for automated DNA preparation and amplification in a single tube.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Mackey, K., Williams, P., Seim, S., and Chomczynski, P. (1996) The use of DNAzol for the rapid isolation of genomic DNA from whole blood.Biomed. Prod. (Suppl.) 13–15.

    Google Scholar 

  2. Chomczynski, P., Mackey, K., Drews, R., and Wilfinger, W. (1997) DNAzol®: a reagent for the rapid isolation of genomic DNA.BioTechniques 22, 550–553.

    PubMed  CAS  Google Scholar 

  3. Cox, R. (1968) The use of guanidium chloride in the isolation of nucleic acids.Methods Enzymol 12(B), 120–129.

    Article  Google Scholar 

  4. Chirgwin, J., Przybyla, R., MacDoinald, R. and Rutter, W. (1979) Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease.Biochemistry 18, 5294–5299.

    Article  PubMed  CAS  Google Scholar 

  5. McCabe, E., Huang, S., Seltzer, W., and Law, M. (1987) DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screening.Human Genet. 75, 213–216.

    Article  CAS  Google Scholar 

  6. Carducci, C., Ellul, L., Antonozzi, I., and Pontecorvi, A. (1992) DNA elution and amplification by polymerase chain reaction from dried blood spots.BioTechniques 13, 735–737.

    PubMed  CAS  Google Scholar 

  7. Jinks, D., Minter, M., Tarver, D., Vanderford, M., Hejtmancik, J., and McCabe, E. (1989) Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening.Human Genet. 81, 363–366.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Karol Mackey.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mackey, K., Steinkamp, A. & Chomczynski, P. DNA Extraction from small blood volumes and the processing of cellulose blood cards for use in polymerase chain reaction. Mol Biotechnol 9, 1–5 (1998). https://doi.org/10.1007/BF02752692

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02752692

Index Entries

Navigation