TEST DIRECTORY

Polymerase chain reaction (PCR)
A technique to amplify a specific target region of DNA in an exponential manner. By heating DNA molecules, the DNA denatures and becomes single stranded, and then by cooling, the DNA anneals to the double stranded again. By using this phenomenon, a single-stranded DNA is used as a template to bind the target primer. The DNA synthesis occurs by repeated cycles of DNA polymerase activity.

Polymerase chain reaction (PCR)
A technique to amplify a specific target region of DNA in an exponential manner. By heating DNA molecules, the DNA denatures and becomes single stranded, and then by cooling, the DNA anneals to the double stranded again. By using this phenomenon, a single-stranded DNA is used as a template to bind the target primer. The DNA synthesis occurs by repeated cycles of DNA polymerase activity.

Polymerase chain reaction (PCR)
A technique to amplify a specific target region of DNA in an exponential manner. By heating DNA molecules, the DNA denatures and becomes single stranded, and then by cooling, the DNA anneals to the double stranded again. By using this phenomenon, a single-stranded DNA is used as a template to bind the target primer. The DNA synthesis occurs by repeated cycles of DNA polymerase activity.

Polymerase chain reaction (PCR)
A technique to amplify a specific target region of DNA in an exponential manner. By heating DNA molecules, the DNA denatures and becomes single stranded, and then by cooling, the DNA anneals to the double stranded again. By using this phenomenon, a single-stranded DNA is used as a template to bind the target primer. The DNA synthesis occurs by repeated cycles of DNA polymerase activity.

Loop-mediated isothermal amplification (LAMP)
LAMP employs 4 kinds of primers that recognize 6 distinct sequences of a target gene. By using the chain substitution reaction, the reaction process proceeds at a constant temperature.

Loop-mediated isothermal amplification (LAMP)
LAMP employs 4 kinds of primers that recognize 6 distinct sequences of a target gene. By using the chain substitution reaction, the reaction process proceeds at a constant temperature.

Loop-mediated isothermal amplification (LAMP)
LAMP employs 4 kinds of primers that recognize 6 distinct sequences of a target gene. By using the chain substitution reaction, the reaction process proceeds at a constant temperature.

Polymerase chain reaction (PCR)
A technique to amplify a specific target region of DNA in an exponential manner. By heating DNA molecules, the DNA denatures and becomes single stranded, and then by cooling, the DNA anneals to the double stranded again. By using this phenomenon, a single-stranded DNA is used as a template to bind the target primer. The DNA synthesis occurs by repeated cycles of DNA polymerase activity.

Real-time PCR
Real-time PCR is the one of the nucleic acid amplification tests using polymerase chain reaction (PCR) as the basic principle. By the use of oligonucleotide that yields fluorescence after degradation, the fluorescent signal is identified for each PCR cycle, which enables the real-time quantification of the target nucleic acid.

Real-time PCR
Real-time PCR is the one of the nucleic acid amplification tests using polymerase chain reaction (PCR) as the basic principle. By the use of oligonucleotide that yields fluorescence after degradation, the fluorescent signal is identified for each PCR cycle, which enables the real-time quantification of the target nucleic acid.

Real-time PCR
Real-time PCR is the one of the nucleic acid amplification tests using polymerase chain reaction (PCR) as the basic principle. By the use of oligonucleotide that yields fluorescence after degradation, the fluorescent signal is identified for each PCR cycle, which enables the real-time quantification of the target nucleic acid.

Transcription-mediated amplification (TMA)
A technique of RNA amplification using two kinds of enzymes, two kinds of primers, and substrates.
Extracted RNA allows reverse transcriptase to create double-stranded DNA. Using the double-stranded DNA as a template, RNA synthesis is repeated by RNA polymerase transcription to amplify the target region of RNA.

Transcription-mediated amplification (TMA)
A technique of RNA amplification using two kinds of enzymes, two kinds of primers, and substrates.
Extracted RNA allows reverse transcriptase to create double-stranded DNA. Using the double-stranded DNA as a template, RNA synthesis is repeated by RNA polymerase transcription to amplify the target region of RNA.

Transcription-mediated amplification (TMA)
A technique of RNA amplification using two kinds of enzymes, two kinds of primers, and substrates.
Extracted RNA allows reverse transcriptase to create double-stranded DNA. Using the double-stranded DNA as a template, RNA synthesis is repeated by RNA polymerase transcription to amplify the target region of RNA.

Transcription-mediated amplification (TMA)
A technique of RNA amplification using two kinds of enzymes, two kinds of primers, and substrates.
Extracted RNA allows reverse transcriptase to create double-stranded DNA. Using the double-stranded DNA as a template, RNA synthesis is repeated by RNA polymerase transcription to amplify the target region of RNA.

Real-time PCR
Real-time PCR is the one of the nucleic acid amplification tests using polymerase chain reaction (PCR) as the basic principle. By the use of oligonucleotide that yields fluorescence after degradation, the fluorescent signal is identified for each PCR cycle, which enables the real-time quantification of the target nucleic acid.

Real-time PCR
Real-time PCR is the one of the nucleic acid amplification tests using polymerase chain reaction (PCR) as the basic principle. By the use of oligonucleotide that yields fluorescence after degradation, the fluorescent signal is identified for each PCR cycle, which enables the real-time quantification of the target nucleic acid.

Real-time PCR
Real-time PCR is the one of the nucleic acid amplification tests using polymerase chain reaction (PCR) as the basic principle. By the use of oligonucleotide that yields fluorescence after degradation, the fluorescent signal is identified for each PCR cycle, which enables the real-time quantification of the target nucleic acid.