Oxford Biosystems

Cytology and Genetics

Cytology and Genetics

Products for cytogenetic investigation and for the detection of genetic variants

Cytology and Genetics

Cytogenetics

The chromosome content of a cell, called karyotype, is classified on the basis of both chromosome number and morphology, which are fixed characteristics for a particular species. The identification and characterisation of either constitutional or acquired chromosome abnormalities, are the focus of two large areas of diagnostic investigation. Cytogenetic analysis is a fundamental tool for prenatal and postnatal diagnosis of several pathologies (concerning general and specialist medicine), and it is the basis of prevention programmes regarding congenital and hereditary diseases.

EuroClone® has developed a perfect combination of media, plastic supports, synchronizing agents, and equipment for pre and postnatal cytogenetic analysis.

Chromosome Media enable simplified operative protocols and produce highly reproducible and readable specimens for microscopic examination. The number of metaphases and chromosome quality are superior compared to conventional media.

  • Chromosome M

    Chromosome Medium M is a complete medium for bone marrow cultures and is supplied in bottles or ready to use culture tubes.

  • Chromosome P

    Chromosome Medium P is a complete medium for peripheral blood cultures and is supplied in bottles (100ml or 500ml) or ready to use culture tubes.

  • SynchroSet

    Synchroset consists of two solutions, which added to the culture medium, and following an extremely simple protocol, allow the synchronization of the cell cycle in both lymphocytes and bone marrow cells. Synchroset is suitable for the production of high numbers of prometaphases in which the chromosomes are appropriate for high resolution banding techniques (up to 850-1000 bands per haploid set). This methodology is suitable for more precise identification of breakpoints and minor abnormalities which often cause severe plurimalformative conditions.

  • ChromoLymphoB Proliferation MIX

    The analysis of chromosomal aberrations of neoplastic cells in patients with haematological disorders provides significant diagnostic and prognostic information. ChromoLympho-B Proliferation MIX, is the mix of ChromoLypmho B Factor and Interleukin 2. ChromoLypmho B Factor is a “new generation” proliferation reagent that, when used in vitro in cultured peripheral blood/bone marrow cells from patients affected with chronic lymphocytic leukaemia (CLL) and other B-cell lymphoproliferative syndromes, has proved a very high success rate of metaphase analysis and an impressive abnormality rate similar to FISH analysis findings.

Genetic variants

ViennaLab Diagnostics has developed a range of products for precise diagnosis. Single and low multiplex markers are targeted with RealFast Assays, and up to 38 genetic variants can be analysed simultaneously with StripAssays®. For comprehensive investigation of numerous genes the Next Generation Sequencing (NGS) assays have been developed.

  • Cancer-Associated Genes

    The identification of somatic pathogenic variants in BRAF, EGFR, KRAS and NRAS genes allows targeted treatment and stratification of cancer patients. Genetic variants of genes involved in drug metabolism (eg DPYD and TMPT) can significantly alter the response to chemotherapeutic treatment.

    ViennaLab Diagnostics offers highly sensitive assays to optimise cancer therapy. Click here for more information.

  • Genetic Disorders

     

  • Genetic abnormalities range from variations in single genes or a group of genes to the gain or loss of an entire chromosome or set of chromosomes. The responsible/causative genetic variants are either inherited from the parents or acquired during a person´s life. ViennaLab provides rapid and robust tests for diagnosis of mono- or polygenic disorders.

  • Genetic Predispositions

    Genetic predisposition is an often inherited genetic change which contributes to the development of a disease but does not directly cause it. Genetic modifiers, lifestyle and environmental factors may increase the risk.

    Several genetic alterations are known to enhance an individual's susceptibility to illnesses like cardiovascular diseases, Alzheimer´s disease, ankylosing spondylitis (Morbus Bechterew) and cancer. Early diagnosis is crucial for timely onset of treatment, maintaining life quality and life expectancy.

  • Microbiome

    Reduced activity or imbalances in the gut microbiome have been associated with a variety of conditions, including obesity, type II diabetes, and many more. ViennaLab 16S Microbiome + ITS NGS Assay, combining library preparation and bioinformatic analysis, enables species-level classification of bacteria and fungi colonizing the human gut.

    Please contact us for information.

  • Pharmacogenetics

    Genetic polymorphisms / aberrations in metabolic pathways often result in an altered response to drugs. Genetic variations in the DNA sequence of drug metabolizing enzymes can substantially influence efficacy and toxicity of drug therapies. ViennaLab offers pharmacogenetic assays to optimize the personalized treatment of the individual patient.

New products are in development for release in 2026. Please contact us for additional information.

Oxford BioSystems

184B Park Drive Milton Park Abingdon Oxon OX14 4SE

Oxford Biosystems has pledged to be an Antibiotic Guardian

members of

BIVDA Member Logo IBMS Company Member