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
01
Testing for Familial Mediterranean Fever and Risk Factors for Amyloidosis
02
Congenital adrenal hyperplasia (CAH) is an inherited disorder of steroid hormone synthesis.
03
Identify the most relevant CFTR mutations and variants for newborn screening and confirmatory genotyping
04
Many people do not have the necessary enzymes in sufficient quantities to digest lactose and fructose.
05
ViennaLab assays identify the most frequent genetic variations responsible for sugar intolerance.
06
ViennaLab assays identify the most relevant genetic variations influencing coumarin anticoagulation therapy.
07
The PGX-TPMT StripAssay® identifies the most frequent polymorphisms in the TPMT gene with therapeutic relevance.
08
The PGX-CYP2C19 StripAssay® detects genetic variants resulting in reduced or increased activity of the cytochrome P450 isoenzyme CYP2C19.
09
The PGX-CYP2D6 StripAssay® detects the most common variants with impaired enzyme activity.
10
The BRAF StripAssays® rapidly identify the most relevant mutations in the BRAF gene.
11
The KRAS and NRAS StripAssays® rapidly identify the most relevant mutations in the KRAS and NRAS genes.
12
The KRAS and NRAS StripAssays® rapidly identify the most relevant mutations in the KRAS and NRAS genes.
13
The EGFR StripAssay® identifies the most important mutations relevant for anti EGFR-TK therapy
14
ViennaLab HLA-B27 assays detect all disease-relevant HLA-B27 subtypes.
15
CVD StripAssays® and RealFast™ Assays identify various combinations of genetic CVD risk factors.
16
Identify the most relevant genetic variations to estimate the risk for Cardiovascular Diseases
17
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.
01
Detects the most common genetic risk factor associated with venous thromboembolism, the 1691G>A mutation in the Factor V (FV) gene
02
Simultaneous detection of the most important thrombophilic mutations 1691G>A in the Factor V gene and 20210G>A in the prothrombin gene
03
Detects the second most important genetic risk factor for venous thromboembolism in the prothrombin (PTH) gene
04
Detect common mutations in the HFE gene causing hereditary haemochromatosis (HH) type 1
05
Simultaneous detection of the two most common mutations in the HFE gene: H63D and C282Y
06
Detects the most common polymorphism in the lactase (LCT) gene causing lactase non-persistence
07
Detect common mutations in the methylenetetrahydrofolate reductase (MTHFR) gene causing hyperhomocysteinemia, which is a risk factor for cardiovascular disease
08
Simultaneous detection of the most common two mutations in the MTHFR gene: 677C>T and 1298A>C
09
Detect common mutations in the methylenetetrahydrofolate reductase (MTHFR) gene causing hyperhomocysteinemia, which is a risk factor for cardiovascular disease
10
Detects the 4G risk allele in the plasminogen activator inhibitor-1 (PAI-1) gene, associated with cardiovascular disease and pregnancy complications
11
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
Detects human leukocyte antigen-B (HLA-B) 5701 allele, which is associated with hypersensitivity to the anti-HIV drug abacavir
13
Detects the human leukocyte antigen-B (HLA-B) 27 allele, which is associated with ankylosing spondylitis
14
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.
