GW thalassemia gDNA reference standard set contains common α and β thalassemia mutations, which can be used as negative and positive controls for daily quality control and performance evaluation of the test process.
● Sample derived from human cell line
Mimic patient samples
● Multiple platforms to verify mutant loci
Sanger sequencing to verify point mutations; GAP-PCR to verify fragment deletions
● Comprehensive variant loci
● Covers common variants of α and β thalassemia
● Negative and positive samples package
28 positive samples + 3 negative samples
● Wide range of applications
PCR, NGS, GeneChip and other platforms are applicable
● Small batch difference, stable and repeatable