TaqPath™ Menu ∣ GeneProof™ Chlamydia trachomatis PCR Kit
TaqPath™ Menu ∣ GeneProof™ Chlamydia trachomatis PCR Kit
Applied Biosystems™

TaqPath™ Menu ∣ GeneProof™ Chlamydia trachomatis PCR Kit

The TaqPath Menu | GeneProof Chlamydia trachomatis PCR Kit enables dual target detection of the 16S rRNA gene and aRead more
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Catalog NumberQuantity
A58121100 reactions kit
Catalog number A58121
Price (EUR)
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Quantity:
100 reactions kit
Price (EUR)
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The TaqPath Menu | GeneProof Chlamydia trachomatis PCR Kit enables dual target detection of the 16S rRNA gene and a cryptic plasmid. 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 Chlamydia trachomatis PCR Kit include:
• High sensitivity secured by targeting multicopy sequence of 16S rRNA gene and dual target detection of 16S rRNA gene and a cryptic plasmid
• Reliable detection of Swedish variant of Chlamydia trachomatis
• Easy to use—single master mix tube containing all components required for PCR amplification
• 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 Chlamydia trachomatis PCR Kit is an in vitro nucleic acid amplification test intended for qualitative detection of Chlamydia trachomatis by real-time polymerase chain reaction (PCR) method. The clinical specimens used for the detection are DNA extracted from swab (cervical, urethral, vaginal), urine, and sperm. The kit can be used in combination with a manual or automated extraction system. It 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

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Available in select countries only.
Specifications
Certification ComplianceCE2797 IVD, Regulation (EU) 2017/746
CompatibilityRegularly tested by QCMD and Instand e.V. External Quality Assessment Panels
Control TemplatePCR inhibition and DNA extraction efficiency control
For Use With (Equipment)QuantStudio™ 3/5 Real-Time PCR System, Applied Biosystems 7300/7500 Real-Time PCR System, StepOne™/StepOne Plus™ Real-Time PCR System, AMPLilab Real-Time PCR System, AriaMx Real-Time PCR System, BioQuant-96 Real-Time PCR System, CFX Connect™/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, LightCycler™ 2.0/480, LineGene 9600/9600 Plus, Mic qPCR Cycler, Rotor-Gene 3000/6000/Q, SLAN™ Real-Time PCR System
No. of Reactions100 reactions
Product LineTaqPath
Quantity100 reactions kit
Sample TypeDNA extracted from swab (cervical, urethral, vaginal), urine, sperm
SensitivityAnalytical: 0.075 cp/μL (Chlamydia trachomatis)Diagnostic: 100% (CI95%: 96.10–100%)
TargetCryptic plasmid and 16S rRNA gene
Target SpecificityAnalytical: 100% (Chlamydia trachomatis including Swedish New Variant and Finnish New Variant of C. trachomatis), Diagnostic: 99.21% (CI95%: 97.50–99.79%)
TechniqueQualitative Analysis
Label or DyeFAM
PCR MethodqPCR
Unit SizeEach
Contents & Storage
• Master mix
• Internal Control
• Positive Control

Store at –20 ± 5°C.