Proven performance of technology as indicated by over 100 peer-reviewed publications.Rapid and accurate sizing enables high throughput identification of premutation carriers access to Xpansion Interpreter® can further refine the risk to full mutation expansion.Detection of challenging allele expansions - including low abundance full mutation size mosaics - provides more sensitive and accurate diagnosis of Fragile X.Highly-sensitive, precise, and accurate assessment of allele size for screening and diagnosis End-to-end solution for FMR1 analysis including all necessary reagents and software.Up to 50-fold reduction in Southern blot analysis.A single multi-allele control provides a peak in every clinical category and can be used as positive control.Reduces valuable operator hands-on-time and overall turnaround time Clinically-validated AmplideX PCR/CE Fragile X Analysis Module automates sample genotyping.Implementation of proprietary PCR solution for amplifying GC-rich regions.Cleared test supports rapid assay validation. To learn more about our complimentary analysis software, click here. The assay also provides access to Asuragen’s Xpansion Interpreter software for the accurate detection of AGG interruptions in the CGG repeat sequence, which allows for a more refined risk assessment for select premutation carriers. The AmplideX Fragile X Dx and Carrier Screen Kit can quickly and effectively be used for either post natal diagnosis or carrier screening for Fragile X Syndrome (FXS). Our Product: The AmplideX Fragile X Dx & Carrier Screen Kit
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