CleanPlex Limb-Girdle Muscular Dystrophy NGS Panel • NUCLEUS BIOTECH

$ 19.50

5 (470) 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.

3D Artificial Skeletal Muscle Constructs Derived from Healthy and

Limb Girdle Muscular Dystrophy Variant Curation Expert Panel - ClinGen

Frontiers Isolation and transfection of myenteric neurons from mice for patch-clamp applications

Limb-Girdle Muscular Dystrophy Scientific Leaders - Together With the FDA - Will Come Together for a Drug Development Workshop on February 8, 2024

Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering - ScienceDirect

Limb-Girdle Muscular Dystrophy Scientific Leaders - Together With the FDA - Will Come Together for a Drug Development Workshop on February 8, 2024

JCI - Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E

Limb-Girdle Muscular Dystrophies

The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease, Orphanet Journal of Rare Diseases

Limb Girdle Muscular Dystrophy Variant Curation Expert Panel - ClinGen

Muscular Dystrophies

Reversal of Defective Mitochondrial Biogenesis in Limb-Girdle Muscular Dystrophy 2D by Independent Modulation of Histone and PGC-1α Acetylation - ScienceDirect

Glycogenin-1 deficiency mimicking limb-girdle muscular dystrophy - ScienceDirect

Molecular mechanisms of muscular dystrophies: old and new players

Limb Girdle Muscular Dystrophy Variant Curation Expert Panel - ClinGen