Development of a Membrane-Based Method for Isolation of Genomic DNA from Human Blood

J Biomol Tech. 2018 Jul;29(2):46-53. doi: 10.7171/jbt.18-2902-001. Epub 2018 Mar 23.

Abstract

High quality and sufficient quantity of genomic DNA (gDNA) are the primary requisites of several molecular biologic applications, including clinical studies related to genetics, genomics, gene polymorphism, and DNA fingerprinting. Whole blood is the primary source of gDNA in most of the clinical investigations. Currently, commercial kits are primarily used to achieve these goals. However, the use of kits is limited by the cost and involvement of several centrifugal steps. Other methods reported are either laborious or do not produce high quality or quantity of gDNA or both. Here, we present the data on the development of a centrifugation-free, cost-effective, and user-friendly method for the isolation of human gDNA from the buffy coat of human blood that involves limited numbers of steps with about 15 min of hands-on time per sample.

Keywords: PCR; buffy coat; centrifugation free; cost effective; gDNA extraction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA / blood
  • DNA / genetics
  • DNA / isolation & purification*
  • DNA Fingerprinting
  • Genome, Human / genetics*
  • Genomics / methods*
  • Humans
  • Polymorphism, Single Nucleotide / genetics

Substances

  • DNA