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The Polymerase Chain Reaction Combined With Quantum Dot Fluorescence Analysis Method for Rapid Detection of Multiple Urinary Tract Infection Pathogens in Children. [PDF]
Li C +6 more
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HMGB1 binds to and disrupts the hairpin structure of RNA15 and inhibits toll-like receptor activation. [PDF]
Lin C +8 more
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Cationic lipid-based nanoparticles for therapeutic delivery in cancer treatment: physicochemical characteristics, therapeutic cargos, and clinical potential. [PDF]
Bae CS, Ahn T.
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Vertical-flow tearable paper-tape rolls for scalable multiplexed point-of-care nucleic acid testing. [PDF]
Shi S +15 more
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Biosensors and Bioelectronics, 2014
Sequence-specific detection of double stranded DNA (dsDNA) is important in various research fields. In general, denaturation of dsDNA into single strands is necessary for the sequence-specific recognition of probes to target DNA, posing several drawbacks which decrease the efficiency as a DNA sensor.
Jieon, Lee +4 more
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Sequence-specific detection of double stranded DNA (dsDNA) is important in various research fields. In general, denaturation of dsDNA into single strands is necessary for the sequence-specific recognition of probes to target DNA, posing several drawbacks which decrease the efficiency as a DNA sensor.
Jieon, Lee +4 more
openaire +4 more sources
The Thermal Denaturation of Desoxyribose Nucleic Acid
Journal of the American Chemical Society, 1957Stuart A. Rice, Paul Doty
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The Alkaline Denaturation of Deoxyribose Nucleic Acid
Journal of the American Chemical Society, 1958Paul Ehrlich, Paul Doty
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Thermal denaturation of nucleic acids in polyacrylamide gels
Analytical Biochemistry, 1974Abstract A system is described for measuring thermal denaturation of nucleic acid fractions directly in polyacrylamide gels. Total nucleic acids were fractionated by disc gel electrophoresis. The buffer within the gel was then exchanged for one commonly used in denaturation studies.
A, Rosner, M, Edelman, J, Gressel
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ChemBioChem, 2004
AbstractIntercalating nucleic acids (INA®s) with insertions of (R)‐1‐O‐(1‐pyrenylmethyl)glycerol were hybridized with locked nucleic acids (LNAs). INA/LNA duplexes were found to be less stable than the corresponding DNA/LNA duplexes when the INA monomer was inserted as a bulge close to the LNA monomers in the opposite strand.
Filichev, V.V. +5 more
openaire +3 more sources
AbstractIntercalating nucleic acids (INA®s) with insertions of (R)‐1‐O‐(1‐pyrenylmethyl)glycerol were hybridized with locked nucleic acids (LNAs). INA/LNA duplexes were found to be less stable than the corresponding DNA/LNA duplexes when the INA monomer was inserted as a bulge close to the LNA monomers in the opposite strand.
Filichev, V.V. +5 more
openaire +3 more sources

