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  1. Removal of small fragments of nucleic acids from plasmid DNA preparations by lithium chloride precipitation The principle of lithium chloride precipitation for removing small fragments of nucleic acids (both DNA and RNA) from plasmid preparations is based on the fact
  2. Removal of ethidium bromide from DNA by ion exchange chromatography Ethidium bromide in DNA purified by cesium chloride gradient centrifugation can be removed by ion-exchange chromatography, followed by ethanol precipitation to
  3. Removal of ethidium bromide from DNA by extraction with organic solvents To remove ethidium bromide from CsCl-gradient purified DNA, repeated extraction with organic solvents is commonly used. Subsequently, CsCl can be removed by dia
  4. Plasmid DNA purification by polyethylene glycol precipitation assay This method was first devised by Richaed Treisman (ICRF, London, UK) with reference to the work of Lis, who was the first to use polyethylene glycol (PEG) to is
  5. Removal of small fragments of nucleic acids from plasmid DNA preparations by NaCl centrifugation Conventional plasmid DNA preparations are contaminated, to varying degrees, with small molecules of DNA or RNA from the genome of the host bacterium or plasmid
  6. Simultaneous Preparation of DNA, RNA and Proteins from Cells and Tissues in a One-Step Process Like the rapid RNA extraction method reported by Chomczynski and Sacchi in 1987, this method consists of lysing cells with a single-phase solution containing gu
  7. Detection of DNA staining in polyacrylamide gels Unlike agarose gels, ethidium bromide cannot be added to polyacrylamide gels as this dye interferes with the polymerization of acrylamide. However, ethidium bro
  8. Transfer and immobilization of denatured RNA on membranes In most cases, to detect a specific target mRNA, the RNA is separated by agarose electrophoresis and then transferred from the gel to a two-dimensional support,
  9. Northern hybridization RNA samples transferred and immobilized to membranes can be hybridized to specific probes that can be used to localize the RNA of interest. Depending on the exp
  10. Dot hybridization and narrow line hybridization of purified RNA The dot and narrow-line hybridization technique (Kafatos et al. 1979) is used to immobilize several nucleic acid samples on the same solid-phase support (usuall
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