An internal PCR control system based on a mouse gene fragment cloned into a vector was developed. The created internal control system allowed for choosing a method for DNA extraction from bio-baits which doesn't inhibit the amplification process when Phytophthora sp. is being diagnosed. During the process of diagnosing the pathogen of the ring rot of potato, it was shown that the developed internal control in real-time PCR turned out to be more informative than the mitochondrial gene of a host plant used for that purpose
AbstractA new marker for rapid and early identification and detection of Phytophthora infestans, the...
The two principal determining steps in molecular diagnosis are the amplification and the identificat...
The aim of this work was to study the Polymerase Chain Reaction (PCR) as a tool of quality control o...
This study aimed to develop a quick and simple method that generates internal controls from any poly...
Phytophthora infestans (mont) de Bary is a pathogen of great concern across the globe, and accurate ...
Conventional methods of pathogen identification have often depended on identification of disease sym...
The ring rot disease of potato, caused by the Gram-positive bacterium, Clavibacter michiganensis sub...
Abstract PCR-based methods were developed for the detection and quantification of the potato pathoge...
Real-time PCR was used for quantitative detection of the potato pathogen, Synchytrium endobioticum, ...
The ribosomal internal transcribed spacer 1 region was sequenced for 10 species of Phythium and eigh...
Lood (x-axis). A, Qiagen DNA mini kit; B, Qiagen M48 DNA mini kit, used on a Qiagen M48 automated DN...
This paper describes a technique for developing a positive control for use in a nested PCR to show t...
A real-time Polymerase Chain Reaction (PCR) system based on Taqman\uae chemistry was developed in or...
Quantitative real-time polymerase chain reaction (qPCR) is a powerful method to compare specific DNA...
Polymerase Chain Reaction (PCR) is a method by which a specific segment of DNA can be replicated for...
AbstractA new marker for rapid and early identification and detection of Phytophthora infestans, the...
The two principal determining steps in molecular diagnosis are the amplification and the identificat...
The aim of this work was to study the Polymerase Chain Reaction (PCR) as a tool of quality control o...
This study aimed to develop a quick and simple method that generates internal controls from any poly...
Phytophthora infestans (mont) de Bary is a pathogen of great concern across the globe, and accurate ...
Conventional methods of pathogen identification have often depended on identification of disease sym...
The ring rot disease of potato, caused by the Gram-positive bacterium, Clavibacter michiganensis sub...
Abstract PCR-based methods were developed for the detection and quantification of the potato pathoge...
Real-time PCR was used for quantitative detection of the potato pathogen, Synchytrium endobioticum, ...
The ribosomal internal transcribed spacer 1 region was sequenced for 10 species of Phythium and eigh...
Lood (x-axis). A, Qiagen DNA mini kit; B, Qiagen M48 DNA mini kit, used on a Qiagen M48 automated DN...
This paper describes a technique for developing a positive control for use in a nested PCR to show t...
A real-time Polymerase Chain Reaction (PCR) system based on Taqman\uae chemistry was developed in or...
Quantitative real-time polymerase chain reaction (qPCR) is a powerful method to compare specific DNA...
Polymerase Chain Reaction (PCR) is a method by which a specific segment of DNA can be replicated for...
AbstractA new marker for rapid and early identification and detection of Phytophthora infestans, the...
The two principal determining steps in molecular diagnosis are the amplification and the identificat...
The aim of this work was to study the Polymerase Chain Reaction (PCR) as a tool of quality control o...