How to become a dealer

If you are interested in becoming our dealer
please contact us

Apply the form

Catalogue

Download

EC CERTIFICATE

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
News & Articles About ILS Our products Advertising materials Contact us
AmpliSens
AmpliSens HPV 16/18-FRT
Cat.: R-V12(RG,iQ,Mx)-CE
Name: AmpliSens HPV 16/18-FRT
Number of tests: 108
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

Information bulletin (version 25.09.2014, update: 02.12.2019)
AmpliSens HPV 16/18-FRT PCR kit Instruction Manual (update 22.07.2021)
Guidelines to AmpliSens HPV 16/18-FRT PCR kit (update 28.07.2021)


AmpliSens HPV 16/18-FRT PCR kit is an in vitro nucleic acid amplification test for qualitative and quantitative detection and differentiation of Human Papillomavirus (HPV) types 16 and 18 DNA in the clinical material (cervical and urethral scrapes) using real-time hybridization-fluorescence detection of amplified products.

Recommended extraction kits: DNA-sorb-AM (K1-12-100-CE), DNA-sorb-C (K1-6-50-CE), DNA-sorb- (K1-2-100-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)
  • iCycler iQ5 (Bio-Rad, USA)
  • Mx3000P or Mx3005P (Stratagene, USA)


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

Back to the section