AltoStar® MERS-CoV RT-PCR Kit 1.5

Order No AS0391543
Rxns 96
Transportation Dry ice
Regulatory status CE-IVD
Mã: AS0391543 Danh mục: Từ khóa:

THÔNG TIN MÔ TẢ

Products not licensed with Health Canada and not FDA cleared or approved. Kits not available in all countries.

The AltoStar® MERS-CoV RT-PCR Kit 1.5 is an in vitro diagnostic test, based on real-time PCR technology, for the qualitative detection of Middle East respiratory syndrome coronavirus (MERS-CoV) specific RNA in human nasopharyngeal swabs. It is intended to be used as an aid for diagnosis of MERS-CoV infection.

Key features

  • Detection of Middle East respiratory syndrome coronavirus (MERS-CoV) specific RNA
  • Consists of two independent assays, one targeting a region upstream of the E gene (upE) as well as a region of the N gene and the other targeting open reading frame 1a (orf1a) of the MERS-CoV genome.
  • CE-IVD marked in vitro diagnostic test
  • Analytical sensitivity reported in copies/ml

Limit of detection (LoD)

LoD upE + N gene 72.9 copies/ml
LoD orf1a 332 copies/ml

Sample types

The following sample type is validated for use with the AltoStar® MERS-CoV RT-PCR Kit 1.5:

  • Human nasopharyngeal swabs

Other workflows

The AltoStar® MERS-CoV RT-PCR Kit 1.5 can be used with compatible workflows (manual or automated). Real-time PCR instruments that have been validated for use with the AltoStar® MERS-CoV RT-PCR Kit 1.5 are:

  • CFX96™ Deep Well Dx System (Bio-Rad)
  • CFX96™ Dx System (Bio-Rad)
  • ABI Prism® 7500 SDS (Applied Biosystems)
  • LightCycler® 480 Instrument II (Roche)
  • QuantStudio™ 5 Real-Time PCR System (Applied Biosystems)
  • Rotor-Gene® Q5/6 plex Platform (QIAGEN)

The AltoStar® MERS-CoV RT-PCR Kit 1.5 can be used with nucleic acid extraction systems other than the AltoStar® AM16. Alternative procedures used for nucleic acid extraction have to be validated by the user.

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