Single tube thalassemia kit

With the thalassemia kit, you can use a single tube of NGS to detect all mutations in HBA1, HBA2, and HBB. This kit detects single nucleotide polymorphisms (SNVs) Indels and CNVs. The extremely simple procedure makes it the best choice for any laboratory, whether you are running advanced secondary genetic testing or large-scale mutation screening. Fast, simple, and powerful NGS workflows replace complex multi-step protocols and eliminate the need to maintain multiple thalassemia tests in your laboratory.