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The SARS-CoV-2 RealFast Assay by ViennaLab Diagnostics GmbH is a diagnostic RT-PCR kit that allows for an accurate and qualitative one-step detection of SARS-CoV-2 sequences in human RNA extracts. This PCR kit also detects the Omikron variant
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The MycoGENIE® Aspergillus species Real-Time PCR kit is a qualitative multiplex PCR that targets sequences of Aspergillus spp. and Mycotypha spp.
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Molzym has one of the best PCR reagents and PCR kits. The products are not only for their fully automated, walk-away system called the SelectNA™plus. But these products can help in all kinds of research.
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The SENTI-GENE ® Pluri CoV-2-FLU-RSV kit is a Real-Time RT-PCR multiplex assay based on nucleic acid amplification for the qualitative detection of SARS-CoV-2, Influenza A and B (Flu A&B) and Human Respiratory Syncytial Virus A&B (RSV) in human respiratory samples. The kit is intended for use as an aid in the differential diagnosis of SARS-CoV-2, Flu A&B and RSV infection in humans.
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The FluCoSyn is a RT-PCR amplification test in a RNA nucleic acid extract designed for the qualitative determination of the presence or absence of the following viruses in one single run: SARS-CoV-2, Influenza (A and B) and Respiratory Syncytial Virus (A and B).
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The ParaGENIE Giardia-Amoeba Real-Time PCR kit is a qualitative quadruplex PCR that targets sequences of Entamoeba histolytica, Entamoeba dispar/moshkovskii and Giardia intestinalis. This kit has been validated on stool (fresh, frozen and fixed) and has a analytical sensitivity of 10 copies for each target.
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The MycoGENIE® Aspergillus fumigatus and resistances TR34/L98H Real-Time PCR kit is a qualitative quadruplex PCR that targets 28s rDNA from Aspergillus fumigatus and TR34/L98H mutations. This kit has been validated on serum, plasma, sputum, BAL, fresh and frozen tissues. It has an analytical sensitivity of 6 copies for the monocopy genes (mutations TR34/L98H) and 1 copy for the multicopy gene (Aspergillus fumigatus rDNA).
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The ParaGENIE Cryptosporidium Microsporidies Real-Time PCR kit is a qualitive quadruplex PCR that targets sequences of Cryptosporidium spp, Enterocytozoon bieneusi and Encephalitozoon intestinalis. Specifically the detection of Cryptosporidium spp. It has an analytical sensitivity of 30 copies for Cryptosporidium spp, 10 copies for Enterocytozoon bieneusi and 20 copies for Encephalitozoon intestinalis.
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TV (Trichomonas vaginalis) is most common by women. Therefore, inclusion in a general CT/NG assay is unnecessary and cost-price ineffective. TV is the responsible pathogen in 5 – 10% of vaginitis cases. In a case of vaginitis where CT/NG are found negative, it is recommended to run a test for TV. This makes the Presto TV PCR the ideal addition to the Presto 100 and Presto 500.
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The Presto 500 Chlamydia and Gonorrhoeae PCR Kit combined qualitative Real-Time assay of Goffin Molecular Technologies is a fast, innovative and robust detection method for sexually transmitted diseases in most human clinical sample materials.
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Sentinel’s STATNAT Line are kits for PCR.
STabilized Amplification Tecnology
STAT-NAT®, the easy way to Nucleic Acid Testing. STAT-NAT® is Sentinel’s proprietary technology that has been developed with a new protective compound able to stabilize the activity of enzymes for a very long time with no temperature controlled storage requirements.
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The MycoGENIE® Pneumocystis jirovecii Real-Time PCR kit is a quantitative duplex PCR that targets the sequence of mitochondrial large sub-unit rRNA. This kit has been validated on sputum and BAL. It has an analytical sensitivity of 4 copies for the mitochondrial gene of Pneumocystis jirovecci.
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The easy RT-PCR kit for COVID-19 detection:
The STAT-NAT ® COVID-19 MULTI is a lyophilized multiplex RT-PCR Real-time PCR qualitative assays based on nucleic acid amplification for the identification of a novel CoronavirusSARS-CoV-2 RNA in human respiratory tract specimens. The assay is an aid in the diagnosis of the SARS-CoV-2 infection (COVID-19).
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Single marker detection. Detects the most common genetic risk factor associated with venous thromboembolism, the 1691G>A mutation in the Factor V (FV) gene.
Multiplex testing. Simultaneous detection of the most important thrombophilic mutations 1691G>A in the Factor V gene and 20210G>A in the prothrombin gene.
Single marker detection. Detects the second most important genetic risk factor for venous thromboembolism in the prothrombin (PTH) gene.
Single marker detection. Detect common mutations in the methylenetetrahydrofolate reductase (MTHFR) gene causing hyperhomocysteinemia, which is a risk factor for cardiovascular disease.
Single marker detection. Detect common mutations in the methylenetetrahydrofolate reductase (MTHFR) gene causing hyperhomocysteinemia, which is a risk factor for cardiovascular disease.
Multiplex testing. Simultaneous detection of the most common two mutations in the MTHFR gene: 677C>T and 1298A>C.
Single marker detection. Identifies patients with the unfavorable TT genotype for Factor XII (FXII), who may have an increased susceptibility to thrombotic disorders.
Single marker detection. Identifies carriers of the protective 34L variant of Factor XIII (FXIII) among at-risk patients of hereditary thrombophilia.
Single marker detection. Detects the human leukocyte antigen-B (HLA-B) 27 allele, which is associated with ankylosing spondylitis. The list of detected alleles can you find here.
Single marker detection. Detects the 4G risk allele in the plasminogen activator inhibitor-1 (PAI-1) gene, associated with cardiovascular disease and pregnancy complications.
Single marker detection. Identifies homozygousity for the -455G>A fibrinogen beta-chain (FGB) allele which may increase susceptibility to atherothrombosis in at-risk patients.
Multiplex testing. Detects *S and *Z variants of the SERPINA1 gene predisposing individuals to chronic obstructive pulmonary disease (COPD) and liver disease due to deficiency of alpha-1 antitrypsin (AAT).
Single marker detection. Detect common mutations in the HFE gene causing hereditary haemochromatosis (HH) type 1.
Single marker detection. Detect common mutations in the HFE gene causing hereditary haemochromatosis (HH) type 1.
Multiplex testing. Simultaneous detection of the two most common mutations in the HFE gene: H63D and C282Y.
Single marker detection. Detects the most common polymorphism in the lactase (LCT) gene causing lactase non-persistence.
Single marker detection. Discriminates between deletions, duplications and normal copy number status of the CYP21A2 gene in patients with CAH.
Single marker detection. Detects a dinucleotide frame-shift variant coding for interleukin 28B (IL28B) and helps to predict the therapeutic response in Hepatitis C Virus infected patients.
Multiplex testing. Simultaneous detection of CYP2C9 *2 (c.430C>T) and CYP2C9 *3 (c.1075A>C) polymorphisms to determine the drug response of coumarin-based anticoagulation therapy.
Single marker detection. Detects a variant in human solute carrier organic anion transporter family member 1B1 (SLCO1B1) gene in patients who are at higher risk for developing statin-induced myopathy.
Single marker detection. Detects the most important polymorphism in the Vitamin K Epoxide Reductase Complex 1 (VKORC1) gene associated with interindividual dose requirements for oral anticoagulants.
Single marker detection. Detects the human leukocyte antigen-A (HLA-A) 3101 allele, which is strongly associated with carbamazepine hypersensitivity reactions in Europeans and Japanese.
Single marker detection. Detects the human leukocyte antigen-B (HLA-B) 1502 allele, which is strongly associated with carbamazepine hypersensitivity reactions in Asian populations.
Single marker detection. Detects human leukocyte antigen-B (HLA-B) 5701 allele, which is associated with hypersensitivity to the anti-HIV drug abacavir.
Liquid Profiling. Detects the T790M mutation in the EGFR gene from cell-free DNA. For monitoring of lung cancer patients who undergo treatment with EGFR tyrosine kinase inhibitors.
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