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EC CERTIFICATE

EC Declaration of Conformity Annex (List B)

EC Declaration of Conformity Annex (Others)

CERTIFICATE ISO 13485

InterLabService
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Phone: +7 (495) 664 2884
Fax: +7 (495) 664 2889

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AmpliSens
AmpliSens Rickettsia conorii-FRT
Cat.: H-2741-1-CE
Name: AmpliSens Rickettsia conorii-FRT
Number of tests: 55
Detection Method: FRT
Packaging arrangement (PA): Kit with reagents only for amplification step
Content: All reagents are in individual vials (no PCR-tubes) + Taq-F polymerase (hot start)
Type: Non-aliquoted
Shelf life: 12 months

Information bulletin to AmpliSens Rickettsia conorii-FRT PCR kit (version 21.03.2018, update: 13.11.2018)
GUIDELINES to AmpliSens Rickettsia conorii-FRT PCR kit (version 19.12.2018, update: 27.12.2018)
AmpliSens Rickettsia conorii-FRT PCR kit Instruction Manual (version 10.09.2019, update: 21.11.2019)


AmpliSens Rickettsia conorii-FRT PCR kit is an in vitro nucleic acid amplification test for qualitative detection of Rickettsia conorii DNA in the biological material (blood, tissue (autopsy, biopsy) material, eschars swabs, cerebrospinal fluid, ticks) using real-time hybridization-fluorescence detection of amplified products.

The PCR kit is used for the analysis of biological material, taken from the persons suspected of tick spotted fever (tick-borne rickettsiosis) without distinction of form and presence of disease manifestation, and ticks.

Recommended extraction kits: RIBO-prep (K2-9-Et-100-CE), MAGNO-sorb (K2-16-200-CE). It is possible to use other nucleic acid extraction protocols.

Adapted for:

  • Rotor-Gene 3000/6000 (Corbett Research, Australia)
  • Rotor-Gene Q (QIAGEN, Germany)
  • CFX96 (Bio-Rad, USA)

 
Attention!!! Number of tests includes controls and calibrators (for quantitative tests).

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