Thalassemia GenoArray Diagnostic Kit
Thalassemia GenoArray Diagnostic Kit
Ref: HBGA-THAL
Thalassemia GenoArray Diagnostic Kit is designed for detection of a-thalassemia and b-thalassemia from each blood sample. Biotinylated primers were designed for specific amplification of a-globin gene deletion/ mutation regions and b-gene deletion/ mutation region respectively.
Amplified DNA amplicons are then hybridized with the immobilized specific thalassemia probes located on the HybriMem under the patented“flow-through hybridization”technique.Enzyme immunoassay method is applied for color development in order to obtain test results to differentiate the patient is whether heterozygous or homozygous thalassemia gene carrier.
Description
Features
- Detection of alpha and beta thalassemia mutation and deletion
- Compatible for use with whole blood, cord blood, dried blood spot and amniotic fluid samples and chorionic villus sample (CVS)
- CE-IVD marked and CFDA registered
- US patented Flow-through Hybridization Technology
- High sensitivity and specificity (compared to CFDA approved kit)
Workflow
Benefits
- Rapid and accurate identification of α & β thalassemia mutations
- Able to differentiate homozygous/heterozygous carrier
- Easy to operate with<2 hours hands-on time
- Effective and cost-efficient