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EC Declaration of Conformity Annex (List B)

EC Declaration of Conformity Annex (Others)

CERTIFICATE ISO 13485

InterLabService
20/13, b.2,
Sadovnicheskaya str.
Moscow, Russia, 115035

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

www.interlabservice.ru sales@ilslab.ru
+7 (495) 664 28 84
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AmpliSens
AmpliSens EBV/CMV/HHV6-screen-FRT
Cat.: R-V48(RG,iQ,Mx)-CE
Name: AmpliSens EBV/CMV/HHV6-screen-FRT
Number of tests: 110
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: 9 months

AmpliSens EBV-CMV-HHV6 Screen Results Matrix v1.02
Information bulletin to AmpliSens EBV / CMV / HHV6-screen-FRT PCR kit (version 20.03.2019, update: 25.03.2019)
AmpliSens EBV / CMV / HHV6-screen-FRT PCR kit Instruction Manual (update 22.07.2021)
Guidelines to AmpliSens EBV / CMV / HHV6-screen-FRT PCR kit (update 28.07.2021)


AmpliSens EBV / CMV / HHV6-screen-FRT PCR kit is an in vitro nucleic acid amplification test for qualitative and quantitative detection of Epstein-Barr virus (EBV) DNA, Human Herpes virus type 6 (HHV6) DNA and human cytomegalovirus (CMV) DNA in clinical materials (whole human blood, white blood cells, viscera biopsy material and cerebrospinal fluid (liquor)) by using real-time hybridization-fluorescence detection of amplified products.

Recommended extraction kit: RIBO-prep (K2-9-Et-100-CE), DNA-sorb-B (K1-2-100-CE). It is possible to use other nucleic acid extraction protocols.

Adapted for:

  • Rotor-Gene 3000, Rotor-Gene 6000 (Corbett Research, Australia)
  • iCycler iQ, iQ5 (Bio-Rad, USA)
  • Mx3000P/Mx3005P (Stratagene, USA)
  • Rotor-Gene Q (QIAGEN, Germany)

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

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