Search Thermo Fisher Scientific
- Contact Us
- Quick Order
-
Don't have an account ? Create Account
Search Thermo Fisher Scientific
Genetic analysis is revolutionizing reproductive health research and transforming the way carrier screening research is being conducted for a healthier future. Genetic analysis is essential to study the genetic disease histories of families and ethnicities with higher rates of genetic disease incidence.
Traditionally, molecular research laboratories have focused on analyzing just a few genetic changes that cause inherited diseases and are known or assumed to be associated with an individual’s ethnicity. With the identification of new causative variants and increasing ethnic diversity, it is more important than ever to include additional variants and diseases in carrier screening research.
Microarray based tools enable comprehensive, efficient, and cost-effective carrier screening studies by analyzing variants across hundreds of genes. It helps to study inherited diseases by consolidating multiple targeted tests on various technology platforms into one test, resulting in quick, comprehensive results.
The Applied Biosystems CarrierScan Assay is an innovative, comprehensive, pan-ethnic and high-throughput microarray-based tool for the reliable and robust detection of sequence and structural variation for carrier screening research across a wide range of ethnicities. The design assesses more variants in each sample, using just one assay to generate reliable, reproducible data in less time compared to traditional single gene testing.
Thermo Fisher Scientific’s simplified carrier screening research workflow allows for increased productivity. With options for manual or automated sample processing protocols, the CarrierScan 1S Assay offers a 96-format plate and can process 3–8 plates per week. The GeneTitan Multi-Channel (MC) Instrument integrates hybridization, fluidics, and imaging and requires less than 30 minutes of hands-on time to operate.
Key benefits for molecular research laboratories:
For Research Use Only. Not for use in diagnostic procedures.