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.
Negative
Pneumocystis carinii (P.jirovecii) DNA
Alveolar lavage fluid
0.7
ARR
(3 month)
3-5
PCR
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.
Negative
Pneumocystis carinii (P.jirovecii) DNA
pleural effusion
0.7
ARR
(3 month)
3-5
PCR
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.
Negative
Pneumocystis carinii (P.jirovecii) DNA
tissue
50mg
ARR
(3 month)
3-5
PCR
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.
Negative
Mycoplasma pneumoniae DNA
Throat swab fluid
ARR
(21 days)
2-4
LAMP
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.
Negative
Mycoplasma pneumoniae DNA
sputum
2
X00
(21 days)
2-4
LAMP
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.
Negative
Legionella DNA Qualitative
sputum
1
X00
(28 days)
3-9
LAMP
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.
Negative
Bordetella pertussis DNA
Posterior nasal swab solution
VS4,ARR
(21 days)
2-4
LAMP
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.
Negative
Entamoeba histolytica DNA qualitative
Feces
0.5g
F00
5-11
PCR
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.
Negative
Gonococcal DNA
Secretion
V50
(28 days)
2-4
PCR (Real Time PCR)
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
Negative
Gonococcal DNA
Partial urine
5
U10
(28 days)
2-4
PCR (Real Time PCR)
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
Negative
Gonococcal DNA
Gargling liquid
5
U10
(28 days)
2-4
PCR (Real Time PCR)
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
Negative
Simultaneous identification of Neisseria gonorrhoeae and Chlamydia trachomatis DNA
Secretion
V50
(28 days)
2-4
PCR (Real Time PCR)
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
Negative
Simultaneous identification of Neisseria gonorrhoeae and Chlamydia trachomatis DNA
Partial urine
5
U10
(28 days)
2-4
PCR (Real Time PCR)
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
Negative
Simultaneous identification of Neisseria gonorrhoeae and Chlamydia trachomatis DNA
Gargling liquid
5
U10
(28 days)
2-4
PCR (Real Time PCR)
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
Negative
Simultaneous nucleic acid detection of Trichomonas vaginalis and Mycoplasma genitalium
Secretion
V50
(28 days)
2-4
PCR (Real Time PCR)
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
Negative
Simultaneous nucleic acid detection of Trichomonas vaginalis and Mycoplasma genitalium
Partial urine
5
U10
(28 days)
2-4
PCR (Real Time PCR)
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
Negative
Virus isolation
See below
V10
4-21
Cytopathic effect, hemocyte adsorption phenomenon, red blood cell agglutination reaction
Virus identification
*See 1
V10
13-29
Neutralization reaction using standard antiserum, immunofluorescence antibody method, hemagglutination inhibition reaction
Simultaneous identification of Neisseria gonorrhoeae and Chlamydia trachomatis rRNA(Suspended beyond orders placed 09-02-2021)
Secretion
V20
2-4
TMA
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.
Negative
Simultaneous identification of Neisseria gonorrhoeae and Chlamydia trachomatis rRNA(Suspended beyond orders placed 09-02-2021)
Partial urine
2.0
V20
(30 days)
2-4
TMA
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.
Negative
Simultaneous identification of Neisseria gonorrhoeae and Chlamydia trachomatis rRNA(Suspended beyond orders placed 09-02-2021)
Gargling liquid
2.0
V20
(30 days)
2-4
TMA
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.
Negative
Mycoplasma pneumoniae DNA Qualitative [QProbe](Suspended beyond orders placed 11-14-2019)
Throat swab fluid
ARR
(28 days)
2-4
PCR(QProbe)
Negative(-)
Simultaneous identification of Neisseria gonorrhoeae and Chlamydia trachomatis rRNA(Suspended beyond orders placed 09-02-2021)
Throat swab fluid
V20
2-4
TMA
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.
Notifications of URL changes/lab information added
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Notifications of URL changes/lab information added
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