Abstract. During the past two decades PCR and several other DNA/RNA amplification techniques have become important diagnostic tools in clinical laboratories. Amplification products contamination has been the main impediment to using these techniques routinely in diagnostic laboratories. Over the years, several creative pre- and post-amplification methods have been developed that prevent amplicon carryover contamination. These procedures, coupled with automated systems that employ real-time amplification and simultaneous detection in a closed system, have substantially reduced the possibility of false positive results due to amplification products carryover contamination. (received 28 July 2004; accepted 15 September 2004
ABSTRACTUse of PCR in the field of molecular diagnostics has increased to the point where it is now ...
This paper describes a technique for developing a positive control for use in a nested PCR to show t...
Frequently, evidentiary items contain an insufficient quantity of DNA to obtain complete or even par...
Contamination of samples with DNA is still a major problem in microbiology laboratories, despite the...
Background: Nucleic acid amplification techniques have become important machineries in the diagnosis...
False-positive results because of carryover contamination by previously amplified nucleic acids are ...
Background\ud The sensitivity of the PCR reaction makes it ideal for use when identifying potentiall...
The polymerase chain reaction (PCR) has revolutionized the detection of DNA and RNA. Real-Time PCR (...
Diagnostic DNA analysis using polymerase chain reaction (PCR) has become a valuable tool for rapid d...
The use of the polymerase chain reaction (PCR) in molecular diagnostics has increased to the point w...
Two-step PCR procedures are an efficient and well established way to generate amplicon libraries for...
Use of PCR in the field of molecular diagnostics has increased to the point where it is now accepted...
Specific diagnostic test results generated by polymerase chain reaction (PCR) depend upon control of...
PCR amplification of minute quantities of degraded DNA for ancient DNA research, forensic analyses, ...
Real-time polymerase chain reaction (RT-PCR) enables effective and sensitive screening for infectiou...
ABSTRACTUse of PCR in the field of molecular diagnostics has increased to the point where it is now ...
This paper describes a technique for developing a positive control for use in a nested PCR to show t...
Frequently, evidentiary items contain an insufficient quantity of DNA to obtain complete or even par...
Contamination of samples with DNA is still a major problem in microbiology laboratories, despite the...
Background: Nucleic acid amplification techniques have become important machineries in the diagnosis...
False-positive results because of carryover contamination by previously amplified nucleic acids are ...
Background\ud The sensitivity of the PCR reaction makes it ideal for use when identifying potentiall...
The polymerase chain reaction (PCR) has revolutionized the detection of DNA and RNA. Real-Time PCR (...
Diagnostic DNA analysis using polymerase chain reaction (PCR) has become a valuable tool for rapid d...
The use of the polymerase chain reaction (PCR) in molecular diagnostics has increased to the point w...
Two-step PCR procedures are an efficient and well established way to generate amplicon libraries for...
Use of PCR in the field of molecular diagnostics has increased to the point where it is now accepted...
Specific diagnostic test results generated by polymerase chain reaction (PCR) depend upon control of...
PCR amplification of minute quantities of degraded DNA for ancient DNA research, forensic analyses, ...
Real-time polymerase chain reaction (RT-PCR) enables effective and sensitive screening for infectiou...
ABSTRACTUse of PCR in the field of molecular diagnostics has increased to the point where it is now ...
This paper describes a technique for developing a positive control for use in a nested PCR to show t...
Frequently, evidentiary items contain an insufficient quantity of DNA to obtain complete or even par...