The importance of copy numbers in genetic diagnostics and research
Copy number variants play a role in many genetic disorders. The fast, accurate and affordable detection of CNVs is essential for clinical genetic testing and research.
MRC Holland develops tools for the detection of DNA copy numbers and methylation patterns associated with disease. Our MLPA technique is the gold standard in this field, and is used around the world to study hereditary disorders and tumours.
Latest News
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Dec 02, 2020Temporary pause in UK shipping
Due to Brexit and the current uncertainty in trade agreements between the UK and EU there will be a pause in shipping to the UK from 1–18 January 2021. For shipment to the UK this year, orders must be received before 15 December 2020.
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Nov 24, 2020MRC Holland holiday closure
MRC Holland will be closed from 25 December 2020 until 1 January 2021. When planning your orders, please keep the following dates in mind:
Last shipping date 2020: Monday 21 December; order deadline: Monday 7 December 2020.
First shipping date 2021: Tuesday 05 January; order deadline: Sunday 20 December 2020.
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Nov 06, 2020First MS-MLPA assay CE-marked: ME011 Mismatch Repair Genes
MRC Holland’s SALSA® MLPA Probemix ME011 Mismatch Repair Genes is the first methylation-specific (MS) MLPA probemix to be CE-marked for in vitro diagnostic use in Europe.
Come and Meet Us
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Jan 26, 2021 - Online (starts 20:00 CET; 11 AM PST; 2 PM EST)
Webinar – Get to Know digitalMLPA
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Feb 17, 2021 - Online (starts 18:00 CET; 9 AM PST; 12 PM EST; 14:00 BRT)
Virtual Workshop – MLPA Raw Data Evaluation and Troubleshooting
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Feb 24, 2021 - Online (starts 14:30 CET; 7 PM IST; 8:30 AM EST; 10:30 BRT)
Virtual Workshop – MLPA Raw Data Evaluation and Troubleshooting
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Nov 01, 2021 - Berlin, Germany
Workshop – Germany (Date TBD)