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VIENNALAB
ViennaLab is proud of its engagement in product development, promoting original IVD StripAssay® and RealFastTM kits worldwide with its existing network of distribution partners, guaranteeing international presence.
ViennaLab Diagnostics offers a variety of easy-to-use in vitro diagnostic kits for the detection of genetic mutations, as well as genetic predispositions, pharmacogenetics and oncology.
ViennaLab StripAssays® and RealFast™ Assays are easy, reliable and affordable – better than any other assay currently on the market.
StripAssays®
Human diagnostic assays for genotyping mutations and polymorphisms (SNPs, deletions, insertions) based on polymerase chain reaction (PCR) and reverse-hybridzation to allele-specific oligonucleotide probes immobilized on teststrips
- Simple and straightforward protocols
- Manual or automated
- Less than 6 hours from DNA to result
- Easy and clear interpretation of results
- Additional mutations readily integrated
- Ready-to-use reagents; inexpensive equipment; CE/IVD labeled kits; sensitive and affordable
01 FMF STRIPASSAY®
Testing for Familial Mediterranean Fever and Risk Factors for Amyloidosis
02 CAH STRIPASSAY®
Congenital adrenal hyperplasia (CAH) is an inherited disorder of steroid hormone synthesis.
03 CF STRIPASSAY®
Identify the most relevant CFTR mutations and variants for newborn screening and confirmatory genotyping
04 LACTOSE INTOLERANCE STRIPASSAY®
Many people do not have the necessary enzymes in sufficient quantities to digest lactose and fructose.
05 SUGAR INTOLERANCE STRIPASSAY®
ViennaLab assays identify the most frequent genetic variations responsible for sugar intolerance.
06 PGX-THROMBO STRIPASSAY®
ViennaLab assays identify the most relevant genetic variations influencing coumarin anticoagulation therapy.
07 PGX-TPMT STRIPASSAY®
The PGX-TPMT StripAssay® identifies the most frequent polymorphisms in the TPMT gene with therapeutic relevance.
08 PGX-CYP2C19 STRIPASSAY®
The PGX-CYP2C19 StripAssay® detects genetic variants resulting in reduced or increased activity of the cytochrome P450 isoenzyme CYP2C19.
09 PGX-CYP2D6 STRIPASSAY®
The PGX-CYP2D6 StripAssay® detects the most common variants with impaired enzyme activity.
10 BRAF 600/601 STRIPASSAY®
The BRAF StripAssays® rapidly identify the most relevant mutations in the BRAF gene.
11 NRAS XL STRIPASSAY®
The KRAS and NRAS StripAssays® rapidly identify the most relevant mutations in the KRAS and NRAS genes.
12 KRAS XL STRIPASSAY®
The KRAS and NRAS StripAssays® rapidly identify the most relevant mutations in the KRAS and NRAS genes.
13 EGFR XL STRIPASSAY®
The EGFR StripAssay® identifies the most important mutations relevant for anti EGFR-TK therapy
14 HLA-B27 STRIPASSAY®
ViennaLab HLA-B27 assays detect all disease-relevant HLA-B27 subtypes.
15 CVD STRIPASSAY® T
CVD StripAssays® and RealFast™ Assays identify various combinations of genetic CVD risk factors.
16 CVD STRIPASSAY® A
Identify the most relevant genetic variations to estimate the risk for Cardiovascular Diseases
17 HAEMOCHROMATOSIS STRIPASSAY® B
ViennaLab assays identify the most common mutations causing iron overload.
RealFast™ Assays
RealFastTM Assays based on real-time PCR detect single nucleotide polymorphisms (SNPs) and copy number variations (CNVs) fast and simply.
- Fast and easy handling
- Same protocol for all genotyping assays
- Less than 90 min from DNA to result
- Controls for wild type and mutant genotypes included
- Compatible with many real-time PCR instruments
Ready-to-use reagents; inexpensive equipment; CE/IVD labeled kits; sensitive and affordable
01 FV LEIDEN REALFAST™ ASSAY
Detects the most common genetic risk factor associated with venous thromboembolism, the 1691G>A mutation in the Factor V (FV) gene
02 FV-PTH MPX REALFAST™ ASSAY
Simultaneous detection of the most important thrombophilic mutations 1691G>A in the Factor V gene and 20210G>A in the prothrombin gene
03 PTH 20210G>A REALFAST™ ASSAY
Detects the most common genetic risk factor associated with venous thromboembolism, the 1691G>A mutation in the Factor V (FV) gene
04 HFE C282Y REALFAST™ ASSAY
Detect common mutations in the HFE gene causing hereditary haemochromatosis (HH) type 1
05 HFE MPX REALFAST™ ASSAY
Simultaneous detection of the two most common mutations in the HFE gene: H63D and C282Y
06 LCT -13910C>T REALFAST™ ASSAY
Detects the most common polymorphism in the lactase (LCT) gene causing lactase non-persistence
07 MTHFR 677C>T REALFAST™ ASSAY
Detect common mutations in the methylenetetrahydrofolate reductase (MTHFR) gene causing hyperhomocysteinemia, which is a risk factor for cardiovascular disease
08 MTHFR MPX REALFAST™ ASSAY
Simultaneous detection of the most common two mutations in the MTHFR gene: 677C>T and 1298A>C
09 MTHFR 1298A>C REALFAST™ ASSAY
Detect common mutations in the methylenetetrahydrofolate reductase (MTHFR) gene causing hyperhomocysteinemia, which is a risk factor for cardiovascular disease
10 PAI-1 4G/5G REALFAST™ ASSAY
Detects the 4G risk allele in the plasminogen activator inhibitor-1 (PAI-1) gene, associated with cardiovascular disease and pregnancy complications
11 SLCO1B1C.521T>C REALFAST™ ASSAY
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
12 HLA-B5701 REALFAST™ ASSAY
Detects human leukocyte antigen-B (HLA-B) 5701 allele, which is associated with hypersensitivity to the anti-HIV drug abacavir
13 HLA-B27 REALFAST™ ASSAY
Detects the human leukocyte antigen-B (HLA-B) 27 allele, which is associated with ankylosing spondylitis
14 EGFR T790M REALFAST™ ASSAY
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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Copyright © 2021 Bi-MEK. All rights reserved.
Copyright © 2020 Bi-MEK. All rights reserved.
Copyright © 2020 Bi-MEK. All rights reserved.