TaqPath™ Menu ∣ GeneProof™ CT/NG/MG Multiplex PCR Kit
Applied Biosystems™

TaqPath™ Menu ∣ GeneProof™ CT/NG/MG Multiplex PCR Kit

The TaqPath Menu | GeneProof CT/NG/MG Multiplex PCR Kit is a real-time PCR testing solution that detects and distinguishes theseMás información
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Número de catálogoCantidad
A581171 kit
Número de catálogo A58117
Precio (CLP)
1.975.400
Each
Cantidad:
1 kit
Precio (CLP)
1.975.400
Each

The TaqPath Menu | GeneProof CT/NG/MG Multiplex PCR Kit is a real-time PCR testing solution that detects and distinguishes these STI pathogens in a single reaction tube: Chlamydia trachomatis, Neisseria gonorrhoeae, and Mycoplasma genitalium. The kit is approved for use on the QuantStudio 5 Real Time PCR System (96-well, 0.2 mL block) and the Applied Biosystems 7500 Real-Time PCR System (96-well).

Features of the TaqPath Menu | GeneProof CT/NG/MG Multiplex PCR Kit include:
• Compatible with other PCR kits in STI workflow
• Easy to use—single master mix tube containing all components required for PCR amplification
• Detects porA mutant of Neisseria gonorrhoeae, Swedish variant of Chlamydia trachomatis, and Finnish New Variant of Chlamydia trachomatis
• High sensitivity—targets the multicopy sequence of 16S rRNA for all three detected pathogens
• Minimizes contamination—the master mix contains uracil-DNA glycosylase (UNG) and dUTPs, reducing carryover contamination
• Compatible with a wide range of real-time PCR devices

The TaqPath Menu | GeneProof CT/NG/MG Multiplex PCR Kit is a real-time PCR testing solution that provides qualitative detection of the most important STI pathogens in a single reaction tube: Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium. The clinical specimens are DNA extracted from swab (cervical, urethral, vaginal) and urine. The kit can be used in combination with a manual or automated extraction system. The kit is intended for diagnostics and aid to diagnosis, and it is designed for professional use in laboratories with trained staff.


Access the Instructions for Use (IFU) approved for your country

Explore more sexually transmitted infections solutions.
For In Vitro Diagnostic Use. Not available in all countries or regions.
Especificaciones
Conformidad de la certificaciónCE2797 IVD / Regulation (EU) 2017/746
CompatibilidadRegularly tested by QCMD and Instand e.V. External Quality Assessment Panels
Molde controlPCR inhibition and DNA extraction efficiency control
Para utilizar con (equipo)QuantStudio™ 5 Real-Time PCR System, Applied Biosystems 7500 Real-Time PCR System, AMPLilab Real-Time PCR System, AriaMx Real-Time PCR System, CFX96™/Dx Real-Time PCR Detection System, CFX Opus 96 Real-Time PCR System, croBEE Real-Time PCR System, Gentier 96E/96R Real-Time PCR System, LineGene 9600 Plus, Mic qPCR Cycler, Rotor-Gene 3000/Q
N.º de reacciones100 reacciones
Línea de productosTaqPath
Cantidad1 kit
Tipo de muestraDNA extracted from swab (cervical, urethral, vaginal), urine
SensibilidadAnalytical: 0.177 cp/μL (Chlamydia), 0.22 cp/μL (Neisseria gonorrhoeae), 1.129 cp/μL (Mycoplasma genitalium), Diagnostic: 100.00% (CI95%: 86.27% – 100.00%) Chlamydia trachomatis, 90.91% (CI95%: 57.12% – 99.52%) Neisseria gonorrhoeae, 100.00% (CI95%: 56.09% – 100.00%) Mycoplasma genitalium
Objetivo16S rRNA gene and cryptic plasmid sequence for Chlamydia trachomatis, 16S rRNA gene and porA pseudogene for Neisseria gonorrhoeae, 16S rRNA gene for Mycoplasma genitalium
Especificidad de diana98.55% (CI95%: 95.48% – 99.62%) Chlamydia trachomatis, 98.24% (CI95%: 95.25% – 99.43%) Neisseria gonorrhoeae, 100.00% (CI95%: 96.40% – 100.00%) Mycoplasma genitalium
TécnicaQualitative Analysis
Método de detecciónqPCR
Etiqueta o tinteFAM
Método de PCRqPCR
Unit SizeEach
Contenido y almacenamiento
• Master mix
• Internal Control
• Positive Control

Store at –20 ± 5°C.