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.
|AAT mpx RealFast Assay||7-265 / 7-268||Multiplex 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 Assay||7-410/—||Single marker detection. Discriminates between deletions, duplications and normal copy number status of the CYP21A2 gene in patients with CAH|
|HFE C282Y RealFast Assay||7-130 / 7-133||Single marker detection. Detect common mutations in the HFE gene causing hereditary haemochromatosis (HH) type 1|
|HFE H63D RealFast Assay||7-140 / 7-143||Single marker detection. Detect common mutations in the HFE gene causing hereditary haemochromatosis (HH) type 1|
|HFE mpx RealFast Assay||7-135 / 7-138||Multiplex testing. Simultaneous detection of the two most common mutations in the HFE gene: H63D and C282Y|
|LCT -13910C>T RealFast Assay||7-150/7-153||Single 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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