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חיפוש מתקדם
Analytical Biochemistry
Gressel, J., Department of Plant Genetics, Weizmann Institute of Science, Rehovot, Israel
Rosner, A., Department of Plant Genetics, Weizmann Institute of Science, Rehovot, Israel
Cohen, N., Department of Plant Genetics, Weizmann Institute of Science, Rehovot, Israel
The electrophoretic mobilities of DNA, ribosomal RNAs, and pulse-labeled RNAs were compared on polyacrylamide gels polymerized at temperatures from 4 to 35°C and subjected to electrophoresis at a fixed temperature. DNA migrated the same distance irrespective of polymerization temperature, the ribosomal RNAs, and the major pulse-labeled species (a putative rRNA precursor) migrated more rapidly in gels polymerized at higher temperatures. The linearity of the migration versus the log of the molecular weight remained for the five rRNA species used, but the extrapolated molecular weight of the putative precursor ranged from 1.8 × 106 to 2.5 × 106 depending on polymerization temperatures. By varying polymerization temperatures, the optimal resolution of various groups of RNA species can be obtained. The results are explained in terms of polymerization temperature effects on gel structure as well as nucleic acid conformation. © 1975.
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תנאי שימוש
Temperature of acrylamide polymerization and electrophoretic mobilities of nucleic acids
69
Gressel, J., Department of Plant Genetics, Weizmann Institute of Science, Rehovot, Israel
Rosner, A., Department of Plant Genetics, Weizmann Institute of Science, Rehovot, Israel
Cohen, N., Department of Plant Genetics, Weizmann Institute of Science, Rehovot, Israel
Temperature of acrylamide polymerization and electrophoretic mobilities of nucleic acids
The electrophoretic mobilities of DNA, ribosomal RNAs, and pulse-labeled RNAs were compared on polyacrylamide gels polymerized at temperatures from 4 to 35°C and subjected to electrophoresis at a fixed temperature. DNA migrated the same distance irrespective of polymerization temperature, the ribosomal RNAs, and the major pulse-labeled species (a putative rRNA precursor) migrated more rapidly in gels polymerized at higher temperatures. The linearity of the migration versus the log of the molecular weight remained for the five rRNA species used, but the extrapolated molecular weight of the putative precursor ranged from 1.8 × 106 to 2.5 × 106 depending on polymerization temperatures. By varying polymerization temperatures, the optimal resolution of various groups of RNA species can be obtained. The results are explained in terms of polymerization temperature effects on gel structure as well as nucleic acid conformation. © 1975.
Scientific Publication
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