New Product: NXtec D028 Carrier Panel 1
We are proud to introduce NXtec D028 Carrier Panel 1 - a high-throughput assay detecting CNVs and selected SNVs for carrier status analysis.
This panel targets genomic regions associated with ten autosomal recessive or X-linked disorders: spinal muscular atrophy (SMA), Duchenne & Becker muscular dystrophy (DMD & BMD), alpha- and beta-thalassemia, cystic fibrosis (CF), congenital adrenal hyperplasia (CAH), DFNB1 hearing loss, juvenile neuronal ceroid lipofuscinoses and cystinosis.
Introductory offer
To celebrate the launch of NXtec D028 Carrier Panel 1, we are offering a 40% discount to first-time digitalMLPA users, valid until August 31st, 2026. Contact us to receive your personal quote.
Are you an existing digitalMLPA user? Then also contact us for an attractive discount!
Key features
• High-specificity: distinguishes even highly homologous regions
• High-throughput: easy integration into existing NGS workflows
• Low cost: < €35 (~US$40-45) reagent costs per sample*
• Fast: <24 h from sample to sequencer, with minimal hands-on time
• Free software included: no bioinformatics expertise required
Coverage
* Costs based on digitalMLPA reagent list prices; possible additional costs not included. Prices may differ when ordering through our sales partners.