PCR solution for COVID-19 and other respiratory diseasesMarket

We have developed a high-quality PCR kit for rapid COVID-19 detection. The protocol is designed for about 60 minutes run time that allows laboratories to deliver the results much faster to patients and doctors. Our break-trough triplex PCR kit of COVID-INFA-INFB will provide fast confirmation of the infection type. All kits are CE IVD certified.

Pipeline

Product / technology
(target/biomarker)
Discovery stageDevelopmentScale-upCommercializationCommercial partner
Proof-of-conceptPre-clinic dataClinical validationCE / IVDRMarket
PCR COVID Kits
(CE IVD)
Progress: 100 %Generi Biotech, Siemens

PCR solution for COVID-19 and other respiratory diseases testing (CE IVD)

GeneSpector provides a wide range of CE IVD kits for detection of SARS-CoV-2 virus (Wuhan coronavirus 2019) based on one-step RT-qPCR using fl uorescently labelled probes. The detection method is based on officially recommended WHO designs for SARS-CoV-2 virus detection and the assessments originate from protocols published by Charité Laboratories (Berlin), Institut Pasteur (Paris) and CDC Laboratories (Atlanta). Our proprietary GEMINI™ probe technology used guarantees the high detection sensitivity.

We offer a fast (65 minutes) protocol under CE-IVD that is suitable for massive testing.

SARS-CoV-2 Influenza A/B

Detection method: one-step real-time PCR

SARS-CoV-2 Influenza A/B CE IVD kit is based on one-step RT-qPCR using fluorescently labelled probes enabling a multiplex detection of viral genes of SARS-CoV-2, Influenza A and Influenza B. The detection method is based on officially recommended WHO and Institut Pasteur designs for detection of SARS-CoV-2 and on usage of our proprietary GEMINI™ probe technology.

Ordering information: 

3233-100 SARS-CoV-2 Influenza A/B – 100 pcs 

3233-500 SARS-CoV-2 Influenza A/B – 500 pcs

 

SARS-CoV-2 Multiplex

Detection method: one-step real-time PCR

Multiplex CE IVD kit for detection of SARS-CoV-2 virus is based on one-step RT-qPCR using fluorescently labelled probes (FAM and HEX channels) and external positive control (Cy5 channel). The detection method is based on officially recommended WHO and Institut Pasteur designs for detection of SARS-Cov-2 and usage of our proprietary GEMINI™ probe technology.

Ordering information: 

3231-050 SARS-CoV-2 Multiplex – 50 pcs

3231-500 SARS-CoV-2 Multiplex – 500 pcs

 

SARS-CoV-2 Combi

Detection method: one-step real-time PCR

Combi CE IVD kit for detection of SARS-CoV-2 virus is based on one-step RT-qPCR using fluorescently labelled probes which allow the detection of viral genes E and RdRP in FAM channel and external positive control in HEX channel. The detection method is based on officially recommended WHO and Institute Pasteur designs for detection of SARS-Cov-2 and usage of our proprietary GEMINI™ probe technology.

Ordering information: 

3232-100 SARS-CoV-2 Combi  – 100 pcs 

3232-500 SARS-CoV-2 Combi  – 500 pcs

 

SARS-CoV-2 Multiplex EndoC

Detection method: one-step real-time PCR

Multiplex CE IVD kit for detection of SARS-CoV-2 virus is based on one-step RT-qPCR using fluorescently labelled probes (FAM and HEX channels) and human endogenous control control (Cy5 channel). The detection method is based on officially recommended WHO and Institut Pasteur designs for detection of SARS-Cov-2 and usage of our proprietary GEMINI™ probe technology.

Ordering information: 

3234-100 SARS-CoV-2 Multiplex EndoC – 100 pcs

3234-500 SARS-CoV-2 Multiplex EndoC – 500 pcs

Contact

GeneSpector s.r.o.
Petrska 1180/3 110 00 Prague, Czech Republic
ID No / IČO: 09404546, file number C 335854
administered by the Municipal Court in Prague

General queries,
investors & partners

info@genespector.com

 

US subsidiary

GeneSpector Innovations USA, Inc.
3500 South Dupont Highway
Dover DE 19901

EU subsidiary

GeneSpector s.r.o.
Petrska 1180/3
110 00 Prague, Czech Republic
ID No / IČO: 09404546
File number C 335854
administered by
the Municipal Court in Prague