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Thalassemia GenoArray Diagnostic kit

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

Amplified DNA amplicons are then hybridized with the immobilized specific thalassemia probes located on the “HybriMem” under the US patented Flow-through Hybridization Technology. Enzyme immunoassay method is applied for color development in order to obtain test results to differentiate whether the patient is heterozygous or homozygous thalassemia gene carrier.

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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 NMPA registered
  • US patented Flow-through Hybridization Technology
  • High sensitivity and specificity (compared to CFDA approved kit)
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