Journal of Clinical Laboratory Analysis · 2017 · 64 citations · 22 references
Life SciencesMolecular BiologyMolecular GeneticsClinical BiochemistryMolecular DiagnosticsNucleic Acid BiochemistryNucleic Acid ExtractionPolymerase Chain ReactionBlood Nucleic Acid ExtractionDna ExtractionDna Extraction EfficiencyPolymerase Chain Reaction Standardization
BACKGROUND: Different methods available for extraction of human genomic DNA suffer from one or more drawbacks including low yield, compromised quality, cost, time consumption, use of toxic organic solvents, and many more. Herein, we aimed to develop a method to extract DNA from 500 μL of fresh or frozen human blood. METHODS: ) were estimated to check the quality and quantity of the extracted DNA sample. Qualitative assessment of the extracted DNA was checked by Polymerase Chain reaction and double digestion of the DNA sample. RESULTS: Our protocol resulted in average yield of 22±2.97 μg and 20.5±3.97 μg from 500 μL of fresh and frozen blood, respectively, which were comparable to many reference protocols and kits. CONCLUSION: Besides yielding bulk amount of DNA, our protocol is rapid, economical, and avoids toxic organic solvents such as Phenol. Due to unaffected quality, the DNA is suitable for downstream applications. The protocol may also be useful for pursuing basic molecular researches in laboratories having limited funds.
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Molecular cloning: A laboratory manual
Prescott L. Deininger · Analytical Biochemistry · 1990 · 86.2K citations
Debomoy K. Lahiri, Steve Bye, John I. Nürnberger et al. · Journal of Biochemical and Biophysical Methods · 1992 · 193 citations