CleanPlex Limb-Girdle Muscular Dystrophy NGS Panel • NUCLEUS BIOTECH
4.5 (568) · $ 15.99 · In stock
NUCLEUS BIOTECH • CleanPlex Limb-Girdle Muscular Dystrophy NGS Panel
The CleanPlex® Limb-Girdle Muscular Dystrophy NGS Panel for Illumina® or Ion Torrent™ is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing (NGS) assay designed to examine the germline variants or mutations across 38 genes associated with Limb-Girdle Muscular Dystrophy. The panel targets all the exonic regions of those genes and the flanking intronic sequences. Compatible with just 10 ng of DNA, sequencing-ready libraries can be prepared using a streamlined workflow in just 3 hours. The pre-designed panel is optimized in silico to deliver data with high on-target performance and high coverage uniformity to ensure efficient use of sequencing reads.
This product is made to order. Once we receive your order, we will synthesize the panel and the kit will contain CleanPlex Multiplex PCR Primers and CleanPlex Targeted Library Kit. CleanPlex Indexed PCR Primers and CleanMag® Magnetic Beads can be ordered separately to complete the workflow from input DNA to sequencing-ready NGS libraries.
You have the option to modify the existing content of this pre-designed panel. Please contact us for a quote.
Interventions for muscular dystrophy: molecular medicines entering the clinic - The Lancet
Limb Girdle Muscular Dystrophy Variant Curation Expert Panel - ClinGen
Limb Girdle Muscular Dystrophy Variant Curation Expert Panel - ClinGen
Limb Girdle Muscular Dystrophy Variant Curation Expert Panel - ClinGen
Limb Girdle Muscular Dystrophy Variant Curation Expert Panel - ClinGen
Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies - Özyilmaz - 2019 - Annals of Human Genetics - Wiley Online Library
Limb-Girdle Muscular Dystrophy Scientific Leaders - Together With the FDA - Will Come Together for a Drug Development Workshop on February 8, 2024
Novel compound heterozygous mutations in the TTN gene: elongation and truncation variants causing limb-girdle muscular dystrophy type 2J in a Han Chinese family
Frontiers Nuclear mechanosignaling in striated muscle diseases
Molecular mechanisms of muscular dystrophies: old and new players
Autosomal Recessive Limb-Girdle Muscular Dystrophies
