Abstract
To simplify our procedure for blood sample processing for PCR, we introduced a simpler, shorter, and more cost-effective method for the separation of peripheral blood lymphocytes (PBL) and DNA extraction for amplification with Taq polymerase. By this method, blood samples are processed in two simple 15-min steps: (1) separation of PBLs from whole blood by red blood cell lysis with the Roche Specimen Washing Solution, and (2) DNA extraction by heat-detergent treatment of separated PBLs. This new method is simpler than the standard Ficoll-Hypaque method for PBLs separation and Proteinase K digestion for DNA extraction. It is not inhibitory to DNA amplification and it allows effective processing of blood samples even after prolonged storage (as long as 8 days) at room temperature. © 1992 by Cold Spring Harbor Laboratory Press.
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CITATION STYLE
Casareale, D., Pottathil, R., & Diaco, R. (1992). Improved blood sample processing for PCR. Genome Research, 2(2), 149–153. https://doi.org/10.1101/gr.2.2.149
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