A method was developed to perform PCR directly on mycelial pellets or colonies treated with NOVOzym 234. The method allows rapid screening of large numbers of transformants of both sporulating and non-sporulating fungi for the presence of (co)transforming plasmid copies or for specific genetic modifications such as gene disruption and site specific integration. PCR fragments of at least 3.2 kb can be obtained. Using this method the identification of specific disruption mutants from Aspergillus niger and Beauveria bassiana was carried out
The paper describes a simple and effective protocol for screening recombinant clones, which can be u...
Colony PCR is a method for rapidly screening colonies of yeast or bacteria that have grown up on sel...
A new and easy polymerase chain reaction (PCR) multiplex strategy, for the identification of the mos...
A quick and reliable method for screening fungal transformants for specific genetic modifications is...
Fungal pure cultures identified with both classical morphological methods and through barcoding sequ...
PCR and DNA sequence analysis have become standard tools for identification, detection and phylogene...
Background: Yeast infections are increasing cause of morbidity and mortality in immunocompromised pa...
Background: Yeast infections are increasing cause of morbidity and mortality in immunocompromised pa...
In this study, a novel rapid and efficient DNA extraction method based on alkaline lysis, which can ...
Research was conducted with laboratory cultures to establish a protocol for the rapid detection and ...
An early diagnosis of an invasive fungal infection is essential for the initiation of a specific ant...
It is estimated that 25 to 50% of the crops harvested worldwide are contaminated with mycotoxins. Be...
The extraction of DNA according to Cenis was used with different modifications of disrupting the cel...
AbstractThe two novel methods for DNA cloning presented here have been developed for the rapid const...
Here, we report on the use of quantitative PCR (qPCR) to determine gene copy number in filamentous f...
The paper describes a simple and effective protocol for screening recombinant clones, which can be u...
Colony PCR is a method for rapidly screening colonies of yeast or bacteria that have grown up on sel...
A new and easy polymerase chain reaction (PCR) multiplex strategy, for the identification of the mos...
A quick and reliable method for screening fungal transformants for specific genetic modifications is...
Fungal pure cultures identified with both classical morphological methods and through barcoding sequ...
PCR and DNA sequence analysis have become standard tools for identification, detection and phylogene...
Background: Yeast infections are increasing cause of morbidity and mortality in immunocompromised pa...
Background: Yeast infections are increasing cause of morbidity and mortality in immunocompromised pa...
In this study, a novel rapid and efficient DNA extraction method based on alkaline lysis, which can ...
Research was conducted with laboratory cultures to establish a protocol for the rapid detection and ...
An early diagnosis of an invasive fungal infection is essential for the initiation of a specific ant...
It is estimated that 25 to 50% of the crops harvested worldwide are contaminated with mycotoxins. Be...
The extraction of DNA according to Cenis was used with different modifications of disrupting the cel...
AbstractThe two novel methods for DNA cloning presented here have been developed for the rapid const...
Here, we report on the use of quantitative PCR (qPCR) to determine gene copy number in filamentous f...
The paper describes a simple and effective protocol for screening recombinant clones, which can be u...
Colony PCR is a method for rapidly screening colonies of yeast or bacteria that have grown up on sel...
A new and easy polymerase chain reaction (PCR) multiplex strategy, for the identification of the mos...