Guangdong Hybribio Biotech Co.,Ltd.

Guangdong Hybribio Biotech Co.,Ltd.

Guangdong,China

Guangdong Hybribio Biotech Co.,Ltd.

Guangdong,China

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Guangdong Hybribio Biotech Co.,Ltd.
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Guangdong Hybribio Biotech Co.,Ltd.

Guangdong,China

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Thalassemia GenoArray Diagnostic Kit

FOB Price : Get a Price/Quote

Min.Order : 1 Piece(s)

Certification : CE

Brand Name : Hybribio

Payment Terms : T/T

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product information

  • brand name : Hybribio

  • certification : CE

  • min.order : 1 Piece(s)

  • warranty : /

  • payment terms : T/T

  • Packaging : /

  • Specification : /

  • place of origin : Guangdong

product description

Introduction
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.  

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)

Experiment Workflow

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Guangdong Hybribio Biotech Co.,Ltd.

Gold verified

Business Type Manufacturer

Country / Region Guangdong,China

Main Products Diagnostic Tests, Laboratory Instruments, Reagents & Chemicals

Main Markets

Thalassemia GenoArray Diagnostic Kit
share :

product information

product description

Introduction
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.  

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)

Experiment Workflow

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