Publication | Open Access
Denaturing Polyacrylamide Gel Electrophoresis
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2000
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EngineeringPolyacrylamide Gel ElectrophoresisMolecular BiologyUniform ThicknessNucleic Acid ChemistryThin Polyacrylamide GelsBioanalysisPolymer Gel ElectrolytesAnalytical ChemistryIsotachophoresisChromatographyDna SequencingCapillary ElectrophoresisOligonucleotideDna ReplicationTypical Sequencing GelBiomolecular EngineeringBiopolymer GelNatural SciencesBiotechnologySynthetic BiologyNucleic Acid AmplificationProtein EngineeringElectrophysiology
Thin polyacrylamide gels that contain a high concentration of urea as a denaturant are capable of resolving short (<500 nucleotides) single-stranded fragments of DNA or RNA that differ in length by as little as one nucleotide. Such gels are uniquely suited for nucleic acid sequence analysis, which is required, for instance, for all footprinting protocols. Thicker gels are often used to purify oligonucleotides. This appendix describes the pouring, running, and processing of a typical sequencing gel, which is 40 cm long with a uniform thickness of 0.4 mm, containing 7 M urea and 4% to 8% acrylamide.
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