When the thymine of T4 DNA is replaced by 5-BU the melting temperature of T4 DNA is increased from about 83° to about 93°C. Heating and slow cooling of T4 DNA at concentrations of about 30μg/ml leads to aggregates which consist of several polynucleotide chains which appear in the electron microscope as a branched structure. The aggregates have regions which are true hybrids. When the concentration of T4 DNA is lowered to less than 1μg/ml the products of hybridization are not aggregates but have the morphology of native DNA molecules and the density labels are distributed as expected from the fusing of two chains of approximately equal length
Hybridization of nucleic acids with secondary structure is involved in many biological processes and...
The effects of enzymatic attack and of shear during the isolation and deproteinization of DNA have b...
Hybridization rates of sheared, genomic E. coli DNA in 0.14 M, pH 6.7 phosphate buffer at 65°C were ...
When the thymine of T4 DNA is replaced by 5-BU the melting temperature of T4 DNA is increased from a...
The design of microarrays is currently based on studies focusing on DNA hybridization reaction in bu...
The thermal stabilities of RNA:DNA hybrids are substantially greater than those of DNA:DNA duplexes ...
How does DNA melt in columnar aggregate relative to its melting in diluted solution? Is the melting ...
A newly developed coarse-grained model called BioModi is utilized to elucidate the effects of temper...
Amplification of DNA in vivo occurs in intracellular environments characterized by macromolecular cr...
The DNA of phage T5 is partially denatured by stirring at 25°C in 0·1 M- or 0·6 M-NaCl at speeds and...
It is well known that multivalent cations can cause DNA to condense from solution to form high-densi...
Rates of formation of RNA:DNA hybrids have been measured as a function of temperature and compared t...
In an accompanying paper we reported the use of differential scanning calorimetry and optical densit...
Under high pH and high salt conditions, Chinese hamster cells lyse and release a DNA-containing mate...
The melting transition of DNA in alkaline CsCl can be followed in the analytical ultra-centrifuge. E...
Hybridization of nucleic acids with secondary structure is involved in many biological processes and...
The effects of enzymatic attack and of shear during the isolation and deproteinization of DNA have b...
Hybridization rates of sheared, genomic E. coli DNA in 0.14 M, pH 6.7 phosphate buffer at 65°C were ...
When the thymine of T4 DNA is replaced by 5-BU the melting temperature of T4 DNA is increased from a...
The design of microarrays is currently based on studies focusing on DNA hybridization reaction in bu...
The thermal stabilities of RNA:DNA hybrids are substantially greater than those of DNA:DNA duplexes ...
How does DNA melt in columnar aggregate relative to its melting in diluted solution? Is the melting ...
A newly developed coarse-grained model called BioModi is utilized to elucidate the effects of temper...
Amplification of DNA in vivo occurs in intracellular environments characterized by macromolecular cr...
The DNA of phage T5 is partially denatured by stirring at 25°C in 0·1 M- or 0·6 M-NaCl at speeds and...
It is well known that multivalent cations can cause DNA to condense from solution to form high-densi...
Rates of formation of RNA:DNA hybrids have been measured as a function of temperature and compared t...
In an accompanying paper we reported the use of differential scanning calorimetry and optical densit...
Under high pH and high salt conditions, Chinese hamster cells lyse and release a DNA-containing mate...
The melting transition of DNA in alkaline CsCl can be followed in the analytical ultra-centrifuge. E...
Hybridization of nucleic acids with secondary structure is involved in many biological processes and...
The effects of enzymatic attack and of shear during the isolation and deproteinization of DNA have b...
Hybridization rates of sheared, genomic E. coli DNA in 0.14 M, pH 6.7 phosphate buffer at 65°C were ...