| Introduction

Genewell thalassemia gDNA reference standard set contains common α and β thalassemia mutations, which can be used as negative and positive controls for routine quality control and performance evaluation of the test process.

| Key Features

● Derived from human cell line 

Mimic clinical samples 

● Multiple platforms to verify mutant loci 

Sanger sequencing to verify point mutations; GAP-PCR to verify fragment deletions

● Matched wildtype and mutation reference standards 

28 positive samples + 3 negative samples

● Comprehensive variant loci 

Covers common variants of α and β thalassemia

● Wide range of applications 

Compatible with PCR, NGS, GeneChip and other platforms 

● Small batch difference, stable and repeatable 

Stable cell lines to ensure consistancy among  batches

| Application

| Product list