New digitalMLPA panels are being added to our portfolio
Advanced panel covering additional genes associated with hereditary cancer syndromes, including CHEK2, PALB2, ATM, and other genes associated with hereditary cancer risk.
More about the panel - https://pentagen.cz/en/produkt/292-nxtec-hereditary-cancer-panel-2-digitalmlpa
A highly discriminatory method for whole-genome analysis of chromosomal abnormalities, targeting regions across all chromosomes, enabling the detection of structural changes such as deletions, duplications, and translocations.
More about the panel - https://pentagen.cz/en/produkt/295-nxtec-karyoprofiler-digitalmlpa
Nxtec D028 Carrier Panel 1
Nxtec D008 DMD
Panel for the analysis of genetic variants associated with autosomal recessive and X-linked disorders included in carrier screening. It enables simultaneous detection of copy number variations (CNVs) and selected single nucleotide variants (SNVs) in a single assay.
More about the panel - https://pentagen.cz/en/produkt/310-nxtec-carrier-panel-1-digitalmlpa?_fid=wof6
A targeted digitalMLPA panel for the reliable detection of copy number variations in the DMD gene associated with Duchenne and Becker muscular dystrophies. It includes two probes for each of the 79 DMD exons and an additional 50 probes distributed across the X chromosome, enabling the detection of both exon-level CNVs and larger chromosomal changes and aneuploidies.
More about tthe panel - https://pentagen.cz/en/produkt/320-nxtectm-d008-dmd
Current product information and related documentation are available on the MRC Holland website.
For more information, please contact us at: diagnostika@pentagen.cz