| Introduction

Duchenne muscular dystrophy (DMD) gDNA reference standard contains common DMD variants in family samples, including deletion and repeats among exons. These reference standards are derived from human cell lines and are ideal for performance validation, DMD assay kit verification and registration, and pedigree sample examinations on multiple nucleic acid detection and NGS platforms.

| Key Features

● Derived from human cell line 

Mimic clinical samples 

● Family sample 

7 familie samples, including common DMD gene deletions  and repeated mutations

● Wide range of applications

PCR-capillary electrophoresis, fluorescent PCR, multiple ligation-dependent probe amplification (MLPA), sequencing

| Application

● Product development and  registration certificate 

Third party reference standards for enterprises

● Routine quality control  

Internal quality and external quality  control for clinical testing

● Methodological  comparison 

Comparing for performance  differences across platforms

● Performance evaluation  of assays 

Kit performance evaluation 

| Product list