Medical Technologies

Neisseria gonorrhoeae DNA Detection Kit in Clinical Samples by PCR with Hybridization-Fluorescence Detection "AmpliPrime Neisseria gonorrhoeae-screen" according to TU 9398-049-09286667-2012

Neisseria gonorrhoeae DNA Detection Kit in Clinical Samples by PCR with Hybridization-Fluorescence Detection "AmpliPrime Neisseria gonorrhoeae-screen" according to TU 9398-049-09286667-2012

The kit for detecting Neisseria gonorrhoeae DNA in clinical material by polymerase chain reaction (PCR) with hybridization-fluorescence detection "AmpliPrime Neisseria gonorrhoeae-screen" according to TU 9398-049-09286667-2012 includes the following components (see attachment on 1 page):

The reagent kit is available in 2 formats:

Format FEP

The reagent kit is available in 3 configurations:

  • Format 1 includes "PCR kit" set FEP variant (0.5 ml tubes).
  • Format 2 includes "PCR kit" set FEP variant (0.2 ml tubes).
  • Format 3 includes "PCR kit" set FEP-1000 variant (0.5 ml tubes).

Format FRT

The reagent kit is available in 3 configurations:

  • Format 1 includes "PCR kit" set FRT variant.
  • Format 2 includes "PCR kit" set FRT-100 F variant.
  • Format 3 includes "PCR kit" set FRT-1000 F variant.

To purchase the Neisseria gonorrhoeae DNA Detection Kit in clinical samples by PCR with hybridization-fluorescence detection "AmpliPrime Neisseria gonorrhoeae-screen" according to TU 9398-049-09286667-2012 (see attachment on 1 page), please fill out a free-form application on our website or use the order form on our site. For more information, contact us via email at Адрес электронной почты защищен от спам-ботов. Для просмотра адреса в вашем браузере должен быть включен Javascript..

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