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FISH signals are enhanced by microwave pulses applied during the DNA-DNAhybridization process.
2
Internal contamination of the implants was evaluated with the checkerboard DNA-DNAhybridization method.
3
This distinction was confirmed by DNA-DNAhybridization and phenotypic tests.
4
It can be differentiated from these species by using phenotypic characteristics, phylogenetic analysis and DNA-DNAhybridization results.
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Results: DNA-DNAhybridization was sensitive enough to detect and quantify the microorganism from the internal parts of the implants.
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These results suggest that quantitative microarray hybridization could be an alternative to conventional DNA-DNAhybridization for measuring chromosome relatedness among bacterial species.
7
DNA-DNA hybridization experiments revealed the presence of three distinct genomospecies and thus confirmed phenotypic differences as revealed by means of extensive biochemical characterization.
8
DNA-DNAhybridization studies revealed a mean hybridization level of 89% between the donkey isolate from California and the donkey isolate from Kentucky.
9
Subgingival plaque samples were taken at each visit and analyzed using the checkerboard DNA-DNAhybridization technique for the presence and levels of 40 subgingival species.
10
The results of DNA-DNAhybridization and the polyphasic data confirmed that strain mano18T can be considered to represent a novel taxon in the genus Stappia.
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Digital DNA-DNAhybridization values between the aforementioned studied strains were well below the 70% threshold for assigning prokaryotic strains to a novel species.
12
On the other hand, the mean DNA-DNAhybridization level from the donkey isolates with DNA from a strain of T. equigenitalis was 23%.
13
The DNA-DNAhybridization experiment showed that there was less than 40 % relatedness between strain CBA1101(T) and the reference species in the genus Halococcus.