Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Multiplex PCR for detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Genitourinary specimens

1 Nov 1995

Abstract excerpt

We developed a multiplex PCR (M-PCR) assay for the simultaneous detection of Chlamydia trachomatis and Neisseria gonorrhoeae. M-PCR employed C. trachomatis-specific primers KL1-KL2 and N. gonorrhoeae-specific primers HO1-HO3 and produced products of 241 and 390 bp, respectively. PCR products were easily detected by agarose gel electrophoresis and confirmed by Southern hybridization using labelled oligonucleotide...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to HIV, Drug Use, Sexual Risk
Share to Reproductive tract infections research
Share to Urinary Tract Infections Management

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8576375
DOI: 10.1128/jcm.33.11.3049-3053.1995

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multiplex PCR for detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Genitourinary specimensPMID 8576375Read ↗

A New Multiplex Genetic Detection Assay Method for the Rapid Semi-Quantitative Detection of Six Common Curable Sexually Transmitted Pathogens From the Genital TractSemantic proximity Read ↗

Highly specific and efficient primers for in-house multiplex PCR detection of Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma hominis and Ureaplasma urealyticumSemantic proximity Read ↗

Characteristics of the m 2000 Automated Sample Preparation and Multiplex Real-Time PCR System for Detection of Chlamydia trachomatis and Neisseria gonorrhoeaeSemantic proximity Read ↗

Quantitative Detection of <i>Mycoplasma genitalium</i> from First-Pass Urine of Men with Urethritis and Asymptomatic Men by Real-Time PCRSemantic proximity Read ↗

Sensitive Simultaneous Detection of Seven Sexually Transmitted Agents in Semen by Multiplex-PCR and of HPV by Single PCRSemantic proximity Read ↗

Use of TaqMan 5′ Nuclease Real-Time PCR for Quantitative Detection of <i>Mycoplasma genitalium</i> DNA in Males with and without Urethritis Who Were Attendees at a Sexually Transmitted Disease ClinicSemantic proximity Read ↗

Detection and Quantification of Mycoplasma genitalium in Male Patients with UrethritisSemantic proximity Read ↗

Development and Validation of a Rotor-Gene Real-Time PCR Assay for Detection, Identification, and Quantification of Chlamydia trachomatis in a Single ReactionSemantic proximity Read ↗

Development and Evaluation of anompAQuantitative Real-Time PCR Assay forChlamydia trachomatisSerovar DeterminationSemantic proximity Read ↗

Novel multiplex real-time PCR system using the SNP technology for the simultaneous diagnosis of Chlamydia trachomatis, Ureaplasma parvum and Ureaplasma urealyticum and genetic typing of serovars of C. trachomatis and U. parvum in NGU.Semantic proximity Read ↗

Comparison of First Void Urine and Urogenital Swab Specimens for Detection of Mycoplasma genitalium and Chlamydia trachomatis by Polymerase Chain Reaction in Patients Attending a Sexually Transmitted Disease ClinicSemantic proximity Read ↗

Polymerase chain reaction-based subtyping of ureaplasma parvum and ureaplasma urealyticum in first-pass urine samples from men with or without urethritis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.