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

Glucose-6-Phosphate Dehydrogenase Deficiency Diagnostic Kit

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a X-chromosomally transmitted disorder of the erythrocyte that affects 400 million people worldwide, occurring with increased frequency througho 2.Detection of 13 mutations on the 6 exons related to G6PD deficiency 3.Compatible for use with whole blood, cord blood, dried blood spot and amniotic fluid samples 4.Include amplification control (IC) and hybridization control (Biotin) for monitoring o
  • Glucose-6-Phosphate Dehydrogenase Deficiency GenoArray Diagnostic Kit

SPECIFICATION

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a X-chromosomally  transmitted disorder of the erythrocyte that affects 400 million people worldwide, occurring with increased frequency throughout Africa, Asia, the Mediterranean, and the Middle East. Prevalence of this deficiency has been found to be the gene mutations that affecting encoding of G6PD, which is correlated with the increased risk of neonatal jaundice,neonatal hyperbilirubinemia and drug or food-induced hem-olytic anemia.

Product Features

1.Detection of 13 mutations on the 6 exons related to G6PD deficiency

2.US patented Flow-through Hybridization Technology

3.Compatible for use with whole blood, cord blood, dried blood spot and amniotic fluid samples

4.Include amplification control (IC) and hybridization control (Biotin) for monitoring of the entire detection process

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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