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.
Negative
Pneumocystis carinii (P. jirovecii) DNA
bronchoalveolar lavage fluid
0.7
ARR
(3 months)
3-5
PCR
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.
Negative
Pneumocystis carinii (P. jirovecii) DNA
pleural fluid
0.7
ARR
(3 months)
3-5
PCR
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.
Negative
Pneumocystis carinii (P. jirovecii) DNA
tissues
50mg
ARR
(3 months)
3-5
PCR
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.
Negative
Mycoplasma pneumoniae DNA
throat swab
ARR
(21 days)
2-4
LAMP
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.
Negative
Mycoplasma pneumoniae DNA
sputum
2.0
X00
(21 days)
2-4
LAMP
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.
Negative
Bordetella pertussis DNA
post-nasal swab
VS4,ARR
(21 days)
2-4
LAMP
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.
Negative
Entamoeba histolytica DNA qualitative
stool
0.5g
F00
5-11
PCR
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.
Negative
Neisseria gonorrhoeae DNA
secretion
V50
(28 days)
2-4
PCR(Real-time PCR)
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.
Negative
Neisseria gonorrhoeae DNA
random urine
5
U10
(28 days)
2-4
PCR(Real-time PCR)
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.
Negative
Neisseria gonorrhoeae DNA
mouth washing liquid
5
U10
(28 days)
2-4
PCR(Real-time PCR)
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.
Negative
Simultaneous identification of rRNA of N. gonorrhoeae and C. trachomatis(Suspended beyond orders placed 09-02-2021)
secretion
V20
2-4
TMA
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.
Negative
Simultaneous identification of rRNA of N. gonorrhoeae and C. trachomatis(Suspended beyond orders placed 09-02-2021)
random urine
2
V20
(30 days)
2-4
TMA
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.
Negative
Simultaneous identification of rRNA of N. gonorrhoeae and C. trachomatis(Suspended beyond orders placed 09-02-2021)
throat swab
V20
2-4
TMA
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.
Negative
Simultaneous identification of rRNA of N. gonorrhoeae and C. trachomatis(Suspended beyond orders placed 09-02-2021)
mouth washing liquid
2
V20
(30 days)
2-4
TMA
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.
Negative
Simultaneous identification of DNA of N. gonorrhoeae and C. trachomatis
secretion
V50
(28 days)
2-4
PCR(Real-time PCR)
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.
Negative
Simultaneous identification of DNA of N. gonorrhoeae and C. trachomatis
random urine
5
U10
(28 days)
2-4
PCR(Real-time PCR)
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.
Negative
Simultaneous identification of DNA of N. gonorrhoeae and C. trachomatis
mouth washing liquid
5
U10
(28 days)
2-4
PCR(Real-time PCR)
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.
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Notifications of URL changes/lab information added
You can now view test items from all labs.
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You can switch between labs as any time using the upper right lab icon.
The domain name of the TEST DIRECTORYpage has changed.
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