• Glucose-6-Phosphate Dehydrogenase Deficiency GenoArray Diagnostic Kit
  • Glucose-6-Phosphate Dehydrogenase Deficiency GenoArray Diagnostic Kit

Thalassemia PCR Diagnostic Kit

1.Detection of alpha and beta thalassemia mutation and deletion 2.Compatible for use with whole blood, cord blood, dried blood spot and amniotic fluid samples and chorionic villus sample (CVS) 3.CE-IVD marked and CFDA registered 4.US patented Flow-through Hybridization Technology 5.High sensitivity and specificity (compared to CFDA approved kit) 
  • Glucose-6-Phosphate Dehydrogenase Deficiency GenoArray Diagnostic Kit

SPECIFICATION

The Hybribio Thalassemia GenoArray Diagnostic Kit is designed for detection of α-thalassemia and β-thalassemia from each blood sample. Biotinylated primers were designed for specific amplification of α-globin gene deletion / mutation regions and β-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.  


Product 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) 



Advantage
1.Rapid and accurate identification of mutations related to G6PD deficiency in one single test

2.Easy to operate with 1 hour hands-on time, result available within 3 hours

3.Simple and direct result interpretation

4.Effective and cost-efficient

5.Able to differentiate homozygous/ heterozygous carrier

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