c trachomatis l2 (ATCC)
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c trachomatis l2
C Trachomatis L2, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 186 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/c+trachomatis/Chlamydia+trachomatis/pm42045288-320-7-10
Average 95 stars, based on 186 article reviews
C Trachomatis L2, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 186 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/c+trachomatis/Chlamydia+trachomatis/pm42045288-320-7-10
Average 95 stars, based on 186 article reviews
c trachomatis l2 - by Bioz Stars,
2026-09
95/100 stars
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other:Article Title: Article Snippet: McCoy cell cultures were used for the recovery of Article Title: Persistence and Significance of Chlamydia trachomatis in the Housefly, Musca domestica L. Article Snippet: We used a human urogenital isolate of Control:Article Title: Development and evaluation of a novel quenching probe PCR (GENECUBE) assay for rapidly detecting and distinguishing between Chlamydia pneumoniae and Chlamydia psittaci. Article Snippet: Early detection of the family Chlamydiaceae as pathogens is essential worldwide for the rapid and sufficient management of atypical pneumonia.. GENECUBE (TOYOBO) is a novel fully automated gene analyzer capable of amplifying and detecting target DNAs within 50 min.. In this study, we developed a new PCR assay with a specific quenching probe (PCR-QC assay) for rapidly distinguishing between Chlamydia pneumoniae (CPN) and Chlamydia psittaci (CPS). Polymerase Chain Reaction:Article Title: Development and evaluation of a novel quenching probe PCR (GENECUBE) assay for rapidly detecting and distinguishing between Chlamydia pneumoniae and Chlamydia psittaci. Article Snippet: Early detection of the family Chlamydiaceae as pathogens is essential worldwide for the rapid and sufficient management of atypical pneumonia.. GENECUBE (TOYOBO) is a novel fully automated gene analyzer capable of amplifying and detecting target DNAs within 50 min.. In this study, we developed a new PCR assay with a specific quenching probe (PCR-QC assay) for rapidly distinguishing between Chlamydia pneumoniae (CPN) and Chlamydia psittaci (CPS). Infection:Article Title: Development and evaluation of a novel quenching probe PCR (GENECUBE) assay for rapidly detecting and distinguishing between Chlamydia pneumoniae and Chlamydia psittaci. Article Snippet: Early detection of the family Chlamydiaceae as pathogens is essential worldwide for the rapid and sufficient management of atypical pneumonia.. GENECUBE (TOYOBO) is a novel fully automated gene analyzer capable of amplifying and detecting target DNAs within 50 min.. In this study, we developed a new PCR assay with a specific quenching probe (PCR-QC assay) for rapidly distinguishing between Chlamydia pneumoniae (CPN) and Chlamydia psittaci (CPS). Positive Control:Article Title: Prevalence of Chlamydia trachomatis, Ureaplasma parvum and Mycoplasma genitalium in Infertile Couples and the Effect on Semen Parameters Article Snippet: DNA amplification was carried out using a thermal cycler (Eppendorf) with a thermal profile as follows: initial denaturation step at 95°C for 5 min, 35 cycles at 95°C for 30 sec, specific annealing temperature mentioned in ( ) for 30 sec, extension step at 72°C for 30 sec followed by a final extension at 72°C for 10 min. Electrophoresis : The PCR products were visualized and photographed under UV light after electrophoresis for 50 min at 100 V through 1.5% agarose gel containing ethidium bromide (1 μg/mL). .. The genomic DNA from Saline:Article Title: Prevalence of Chlamydia trachomatis, Ureaplasma parvum and Mycoplasma genitalium in Infertile Couples and the Effect on Semen Parameters Article Snippet: DNA amplification was carried out using a thermal cycler (Eppendorf) with a thermal profile as follows: initial denaturation step at 95°C for 5 min, 35 cycles at 95°C for 30 sec, specific annealing temperature mentioned in ( ) for 30 sec, extension step at 72°C for 30 sec followed by a final extension at 72°C for 10 min. Electrophoresis : The PCR products were visualized and photographed under UV light after electrophoresis for 50 min at 100 V through 1.5% agarose gel containing ethidium bromide (1 μg/mL). .. The genomic DNA from Negative Control:Article Title: Prevalence of Chlamydia trachomatis, Ureaplasma parvum and Mycoplasma genitalium in Infertile Couples and the Effect on Semen Parameters Article Snippet: DNA amplification was carried out using a thermal cycler (Eppendorf) with a thermal profile as follows: initial denaturation step at 95°C for 5 min, 35 cycles at 95°C for 30 sec, specific annealing temperature mentioned in ( ) for 30 sec, extension step at 72°C for 30 sec followed by a final extension at 72°C for 10 min. Electrophoresis : The PCR products were visualized and photographed under UV light after electrophoresis for 50 min at 100 V through 1.5% agarose gel containing ethidium bromide (1 μg/mL). .. The genomic DNA from |
