We are an EN ISO 13485 certified EU-located company developing and producing CE IVD real-time PCR kits.
Our in vitro diagnostics fall into five categories: clinical genetics, hematology, pharmacogenetics, oncology and microbiology.
Our typical partners are end-users of the RT-PCR kits (mostly in CZ and SK), business partners and distributors. We are looking for business partners and/or distributors worldwide who can fit the portfolio of our products, either the whole or a part of it, to their sales strategy (see here).
gb HEMO FV (G1691A) The CE IVD real-time PCR kit is intended for detection of mutation G1691A (Leiden) in coagulation factor V in human genomic DNA. Detection is based on real-time polymerase chain reaction (qPCR) using fluorescently labelled probes (allelic discrimination).
gb HEMO FII (G20210A) The CE IVD real-time PCR kit is intended for detection of mutation G20210A in coagulation factor II in human genomic DNA. Detection is based on real-time polymerase chain reaction (qPCR) using fluorescently labelled probes (allelic discrimination).
gb HEMO MTHFR (C677T) The CE IVD real-time PCR kit is intended for detection of mutation C677T in MTHFR gene in human genomic DNA. Detection is based on real-time polymerase chain reaction (qPCR) using fluorescently labelled probes (allelic discrimination).
gb HEMO MTHFR (A1298C) The CE IVD real-time PCR kit is intended for detection of mutation A1298C in MTHFR gene in human genomic DNA. Detection is based on real-time polymerase chain reaction (qPCR) using fluorescently labelled probes (allelic discrimination).
gb GENETIC Gilbert The CE IVD real-time PCR kit is intended for detection of polymorphism TA (allele 7TA) in gene UGT1A1 in human genomic DNA. Detection is based on polymerase chain reaction (PCR) with analysis of melting curves using fluorescently labelled probe.
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