Protocol Exchange · 2016 · 17 citations · 0 references
Life SciencesBiotechnologyPlant SciencesNucleic Acid BiochemistryPlant BiotechnologyPlant Molecular BiologyExtraction TechniquesIsolation ProceduresMetabolite ExtractionNucleic Acid ExtractionNucleic Acid PurificationRibonucleic Acid (Rna) ChemistryDna ExtractionHigh-purity Nucleic Acid RecoveryPlant Nucleic Acid ExtractionRibonucleic Acid ExtractionRna ExtractionSecondary MetabolitesTissue Nucleic Acid ExtractionTotal Nucleic Acid Extraction
This protocol describes a rapid DNA and RNA extraction method for plant tissues.Hexadecyltrimethylammonium bromide (CTAB), sodium chloride (NaCl), tris base, and ethylenediaminetetraacetic acid (EDTA) are the main components of the extraction buffer.In contrast to all previously reported protocols, this extraction method does not require any stock solutions.This isolation buffer is potential of extracting both DNA and RNA simultaneously.Depending on the purpose of the project, the corresponding steps can be slightly altered to obtain either DNA or RNA.The big advantage of this method is to use general laboratory chemicals to make a powerful extraction buffer, resulting in high quality and quantity nucleic acid.Also, CTAB in this buffer is capable of isolating nucleic acid from recalcitrant plants enriched in secondary metabolites.Importantly, this method is recommended for the projects at which isolating nucleic acid in a short time is of crucial importance.This method probably is usable for all plant tissues and takes about an hour.