The table below shows the RealFast Assays that are related to Genetic disorders. You can find the manual of the RealFast Assay by each reference number. The available brochures can be found under the headline product.

ProductReference
100/32reactions
Application
AAT deficiency/COPD
AAT mpx RealFast Assay7-265 / 7-268Multiplex testing. Detects *S and *Z variants of the SERPINA1 gene predisposing individuals to chronic obstructive pulmonary disease (COPD) and liver disease due to deficiency of alpha-1 antitrypsin (AAT)
Congenital Adrenal Hyperplasia
CAH RealFast Assay7-410/—Single marker detection. Discriminates between deletions, duplications and normal copy number status of the CYP21A2 gene in patients with CAH
Haemochromatosis
HFE C282Y RealFast Assay7-130 / 7-133Single marker detection. Detect common mutations in the HFE gene causing hereditary haemochromatosis (HH) type 1
HFE H63D RealFast Assay7-140 / 7-143Single marker detection. Detect common mutations in the HFE gene causing hereditary haemochromatosis (HH) type 1
HFE mpx RealFast Assay7-135 / 7-138Multiplex testing. Simultaneous detection of the two most common mutations in the HFE gene: H63D and C282Y
Carbohydrate Intolerance
LCT -13910C>T RealFast Assay7-150/7-153Single marker detection. Detects the most common polymorphism in the lactase (LCT) gene causing lactase non-persistence

Click here for StripAssays related to genetic disorders. 

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