Adellgene®

Adellgene® line is a products range based on fragment analysis technology, in which DNA is amplified by conventional PCR and separated by capillary electrophoresis in a genetic sequencer. This technology allows to quantify the number of triplet repeats so as to classify genotypically a given sample. This product line is focused on rare diseases, being a very good CE solution for genetic laboratories.

Adellgene® RED 1000

Adellgene® RED 1000 is a DNA size standard that provides single-stranded, ROX-labeled fragments in the 50-1000 bp range.

Adellgene® Fragile X

Kit for the determination of healthy, intermediate, premutation and mutant alleles in the FMR1 gene by fluorescent fragment analysis

Adellgene® Fragile X Screening

Kit for the determination of healthy and premutation alleles in the FMR1 gene by fluorescent fragment analysis

Adellgene® Friedreich’s Ataxia

Kit for the determination of the GAA triplet repeats number of the FXN gene by fluorescent fragment analysis

Adellgene® Huntington Disease

Kit for the determination of the CAG triplet repeats number of the HTT gene by fluorescent fragment analysis

Adellgene® SCAs

Kit for the determination of the number of triplets in the genes ATXN1 (SCA1), ATXN2 (SCA2), ATXN3 (SCA3), CACNA1A (SCA6), ATXN7 (SCA7), PPP2R2B (SCA12), TBP (SCA17) and ATN1 (DRPLA), by fragment analysis.

Adellgene® Myotonic Dystrophy Confirmatory

Kit for the determination of the CTG triplet repeats number of the DMPK gene by fluorescent fragment analysis

Adellgene® Myotonic Dystrophy Screening

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Kit for the determination of the CTG triplet repeats number of the DMPK gene by fluorescent fragment analysis

About Adellgene®

BDR and Adellgene® are part of Orphanet, a global multi-stakeholder consortium from 41 countries, which aims to provide high quality information on rare diseases and to ensure equitable access to knowledge for all stakeholders.

Orphanet is a unique resource that gathers and updates knowledge on rare diseases in order to improve the diagnosis, care and treatment of patients with rare diseases.

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