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Thalassemia GenoArray Diagnostic Kit

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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