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Quidel™ Lyra RSV+hMPV Molecular Assay

Multiplex RT-PCR assay for qualitative detection/ID of respiratory syncytial virus/human metapneumovirus viral RNA extracted from nasal/nasopharyngeal swab specimens, FDA approved for use on Applied Biosystems™ 7500 FastDx RT-PCR, QuantStudioDx RT-PCR, Cepheid™ SmartCycler™ II

Manufacturer:  Quidel™ M103

Catalog No. 23-044-002


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Description

Description

  • RT-PCR
  • One-step reagent setup
  • Results in <70 minutes after extraction
  • No freezer necessary
  • Refrigration storage
  • Long shelf-life
  • Flexible testing format
  • Includes 12 x 8 master mix, rehydration solution and liquid process controls
Specifications

Specifications

FDA approved*
Included
Yes
Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) ribonucleic acid (RNA)
Molecular Testing
Group A β-hemolytic Streptococcus 96%, Pyogenic Group C and G β-hemolytic Streptococcus 95%, Positive Percent Agreement: hMPV: 98.0%
RT-PCR
Tests and controls
96 Tests/Kit
<70 min. after extraction
2°C to 8°C
Qualitative detection and identification of respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) ribonucleic acid (RNA) extracted from nasal and nasopharyngeal swab specimens from patients with signs and symptoms of respiratory infection
Highly Complex
No
Throat swab specimens obtained from patients symptomatic of acute pharyngitis
Molecular Testing
FDA approved for use on Applied Biosystems™ 7500 Fast Dx Real-Time PCR Instrument, QuantStudioTM Dx Real-Time PCR Instrument and Cepheid™ SmartCycler™ II
Kit
Group A β-hemolytic Streptococcus 98%, Pyogenic Group C and G β-hemolytic Streptococcus 1.8x104 CFU/mL, Negative Percent Agreement: hMPV: 98.9%
Safety and Handling

Safety and Handling

ShelfLife : 2 Years from DOM

SDS
Documents

Documents

Product Certifications
Promotions

Promotions

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