Genetics
The AmplideX suite of products is designed to solve unmet testing needs in inherited genetic disorders. The technology overcame a 20-year challenge by reliably amplifying the FMR1 gene. This allowed researchers to gain a deeper understanding of fragile X syndrome, the most commonly known inherited cause of intellectual disability and autism.
Asuragen pioneered innovation in three major areas:
- Reduced Complexity
Amplification and analysis of GC-rich and high homology target sequences - Optimised Workflow
Assay and informatics solutions to optimise efficiency, hands-on time and cost - Quality Performance
Accuracy, sensitivity, specificity and reproducibility with FMR1
Filter results:
Portfolio | Code | //= _e('Incubation', 'prodotto');?>Classification | Clinical Area | ||
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AmplideX FMR1 mPCR Kit (Metilazione) |
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49442 | RUO | Genetics |
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AmplideX FMR1 PCR Process Control |
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49513 | RUO | Genetics |
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AmplideX FMR1 Methylation & Sensitivity Control |
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49514 | RUO | Genetics |
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AmplideX PCR/CE C9ORF72 KIT |
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49581 | RUO | Genetics |
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AmplideX PCR/CE HTT KIT |
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49657 | RUO | Genetics |
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AmplideX FMR1 PCR KIT |
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76008 | IVD CE FDA | Genetics |
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AmplideX DM1 DX KIT |
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76048 | IVD CE | Genetics |
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AmplideX SMA PLUS KIT |
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A00055 - A00056 | IVD CE | Genetics |
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