TEST DIRECTORY

PCR (Polymerase chain reaction)
Uses the fact that DNA dissociates from double strands to single strands when heated and returns to double strands when cooled, and binds the desired primer using single stranded DNA as a template. A method in which the target DNA region is exponentially amplified by repeatedly performing DNA synthesis using the transcription reaction of DNA polymerase.

PCR (Polymerase chain reaction)
Uses the fact that DNA dissociates from double strands to single strands when heated and returns to double strands when cooled, and binds the desired primer using single stranded DNA as a template. A method in which the target DNA region is exponentially amplified by repeatedly performing DNA synthesis using the transcription reaction of DNA polymerase.

PCR (Polymerase chain reaction)
Uses the fact that DNA dissociates from double strands to single strands when heated and returns to double strands when cooled, and binds the desired primer using single stranded DNA as a template. A method in which the target DNA region is exponentially amplified by repeatedly performing DNA synthesis using the transcription reaction of DNA polymerase.

PCR (Polymerase chain reaction)
Uses the fact that DNA dissociates from double strands to single strands when heated and returns to double strands when cooled, and binds the desired primer using single stranded DNA as a template. A method in which the target DNA region is exponentially amplified by repeatedly performing DNA synthesis using the transcription reaction of DNA polymerase.

LAMP (Loop-Mediated Isothermal Amplification)
A method in which four types of primers are set for six regions from the target gene sequence and reacted at a constant temperature using strand displacement reaction.

LAMP (Loop-Mediated Isothermal Amplification)
A method in which four types of primers are set for six regions from the target gene sequence and reacted at a constant temperature using strand displacement reaction.

LAMP (Loop-Mediated Isothermal Amplification)
A method in which four types of primers are set for six regions from the target gene sequence and reacted at a constant temperature using strand displacement reaction.

LAMP (Loop-Mediated Isothermal Amplification)
A method in which four types of primers are set for six regions from the target gene sequence and reacted at a constant temperature using strand displacement reaction.

PCR (Polymerase chain reaction)
Uses the fact that DNA dissociates from double strands to single strands when heated and returns to double strands when cooled, and binds the desired primer using single stranded DNA as a template. A method in which the target DNA region is exponentially amplified by repeatedly performing DNA synthesis using the transcription reaction of DNA polymerase.

Real-time PCR
A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

Real-time PCR
A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

Real-time PCR
A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

Real-time PCR
A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

Real-time PCR
A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

Real-time PCR
A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

Real-time PCR
A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

Real-time PCR
A type of nucleic acid amplification method based on the basic principle of PCR, which uses oligonucleotides that emit fluorescence upon decomposition to quantify target nucleic acids in real time by checking the fluorescent signal at each PCR cycle. A measurement method that enables

TMA (Transcription mediated amplification)
A method of amplifying RNA using two types of enzymes and two types of primers and substrates.
Double-stranded DNA is synthesized from the extracted RNA using reverse transcriptase, and this double-stranded DNA is used as a template to synthesize RNA by RNA polymerase transcription reaction, which is repeated to amplify the desired RNA region.

TMA (Transcription mediated amplification)
A method of amplifying RNA using two types of enzymes and two types of primers and substrates.
Double-stranded DNA is synthesized from the extracted RNA using reverse transcriptase, and this double-stranded DNA is used as a template to synthesize RNA by RNA polymerase transcription reaction, which is repeated to amplify the desired RNA region.

TMA (Transcription mediated amplification)
A method of amplifying RNA using two types of enzymes and two types of primers and substrates.
Double-stranded DNA is synthesized from the extracted RNA using reverse transcriptase, and this double-stranded DNA is used as a template to synthesize RNA by RNA polymerase transcription reaction, which is repeated to amplify the desired RNA region.

TMA (Transcription mediated amplification)
A method of amplifying RNA using two types of enzymes and two types of primers and substrates.
Double-stranded DNA is synthesized from the extracted RNA using reverse transcriptase, and this double-stranded DNA is used as a template to synthesize RNA by RNA polymerase transcription reaction, which is repeated to amplify the desired RNA region.

TMA (Transcription mediated amplification)
A method of amplifying RNA using two types of enzymes and two types of primers and substrates.
Double-stranded DNA is synthesized from the extracted RNA using reverse transcriptase, and this double-stranded DNA is used as a template to synthesize RNA by RNA polymerase transcription reaction, which is repeated to amplify the desired RNA region.

TMA (Transcription mediated amplification)
A method of amplifying RNA using two types of enzymes and two types of primers and substrates.
Double-stranded DNA is synthesized from the extracted RNA using reverse transcriptase, and this double-stranded DNA is used as a template to synthesize RNA by RNA polymerase transcription reaction, which is repeated to amplify the desired RNA region.