The purpose of the work: the development of the molecular-biological methods of identification. Obtained has been the probe for the DNA-hybridization, specific for the gene of neurotoxin C.botulinum of type A. Developed has been the specific and sensitive enough (5 ng DNA) method of the DNA-hybridization, allowing to reveal the presence of the neurotoxin gene, type A. Using the method of hybridization by Sauzern, first it has been shown, that two groups of strains, type A, having the different fields of DNA before the strating codon of the neurotoxin gene, exist. The PCR method for identification of C.botulinum, types A and B, has been developed; the high specificity and sensitivity (1 pg DNA) of this method have been shown. It has been sho...
The purpose of the work: constructing the DNA-probes and working the optimum conditions of its appli...
A stretch of the 23S rDNA from Clostridium botulinum strains that produce different types of neuroto...
Amplified fragment length polymorphism (AFLP) analysis was applied to characterize 33 group I and 37...
The polymerase chain reaction (PCR) was used as the basis for the development of highly sensitive an...
Specific primers for C. botulinum types A and E neurotoxin genes were evaluated both from the litera...
The application of the polymerase chain reaction (PCR) for detection of Clostridium botulinum types ...
Botulism is diagnosed by detecting botulinum neurotoxin and Clostridium botulinum cells in the patie...
In the development of new food products, more knowledge is needed about the occurrence and quantity ...
Clostridium botulinum types C and D, as well as their mosaic variants C-D and D-C, are associated wi...
This study was undertaken to examine phenotypic and genetic features of strains preliminary classifi...
PCR for the detection of botulinum neurotoxin gene types A to E was used in the investigation of a c...
Groups I (proteolytic) and II (nonproteolytic) C. botulinum are genetically and physiologically dist...
Botulinum neurotoxins are produced by the anaerobic bacterium Clostridium botulinum and are divided ...
We report the development of real-time PCR assays for genotyping Clostridium botulinum group III tar...
AIMS: An immuno-polymerase chain reaction (immuno-PCR) has been developed for the sensitive detectio...
The purpose of the work: constructing the DNA-probes and working the optimum conditions of its appli...
A stretch of the 23S rDNA from Clostridium botulinum strains that produce different types of neuroto...
Amplified fragment length polymorphism (AFLP) analysis was applied to characterize 33 group I and 37...
The polymerase chain reaction (PCR) was used as the basis for the development of highly sensitive an...
Specific primers for C. botulinum types A and E neurotoxin genes were evaluated both from the litera...
The application of the polymerase chain reaction (PCR) for detection of Clostridium botulinum types ...
Botulism is diagnosed by detecting botulinum neurotoxin and Clostridium botulinum cells in the patie...
In the development of new food products, more knowledge is needed about the occurrence and quantity ...
Clostridium botulinum types C and D, as well as their mosaic variants C-D and D-C, are associated wi...
This study was undertaken to examine phenotypic and genetic features of strains preliminary classifi...
PCR for the detection of botulinum neurotoxin gene types A to E was used in the investigation of a c...
Groups I (proteolytic) and II (nonproteolytic) C. botulinum are genetically and physiologically dist...
Botulinum neurotoxins are produced by the anaerobic bacterium Clostridium botulinum and are divided ...
We report the development of real-time PCR assays for genotyping Clostridium botulinum group III tar...
AIMS: An immuno-polymerase chain reaction (immuno-PCR) has been developed for the sensitive detectio...
The purpose of the work: constructing the DNA-probes and working the optimum conditions of its appli...
A stretch of the 23S rDNA from Clostridium botulinum strains that produce different types of neuroto...
Amplified fragment length polymorphism (AFLP) analysis was applied to characterize 33 group I and 37...