Education
Learn more about MLPA by using our free e-learning modules, general videos and Coffalyser.Net videos. For our MLPA workshops, see here.

E-learning

MLPA Quality Control fragments
Learn how to use the Quality Control fragments to assess the quality of your MLPA experiments.

MLPA Quality Control fragments
This module is available in the following languages: English and German.

MLPA Troubleshooting Wizard
This interactive Wizard helps you to quickly troubleshoot potential problems in your MLPA reactions.

MLPA troubleshooting wizard

Internet Explorer users: version 9 or higher is required to be able to view our E-learning modules and Troubleshooting Wizard.

General videos
MLPA® is the gold standard for DNA copy number quantification and is used to study both hereditary disorders and tumours. This animation explains how the MLPA technique works.

How does MLPA work?

This video teaches you how to perform an MLPA reaction in the lab.

How to perform an MLPA reaction


Coffalyser.Net videos
This video shows you how to create a manual bin set in Coffalyser.Net.

How create a manual bin set in Coffalyser.Net

This video shows you how to add Coffalyser sheets to the sheet library in Coffalyser.Net.

How to add Coffalyser sheets to the sheet library
new products
P484-ALPL
Hypophosphatasia (HPP)
P474-CD274-PDCD1LG2-JAK2
Various cancer types
P480-WHS & Achondroplasia
Wolf Hirschhorn Syndrome, Achondroplasia
P478-SMARCE1
Meningioma, Coffin-Siris syndrome
improved products
P021-SMA
Spinal muscular atrophy (SMA)
P128-CYP450
Cytochrome P450
P225-PTEN
PTEN hamartoma tumor syndrome, Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN-related proteus syndrome, Proteus-like syndrome; (Tumour analysis for research use only)
P072-MSH6-MUTYH
Lynch syndrome; MUTYH-associated polyposis (MAP)
P158-JPS
Juvenile polyposis syndrome (JPS)
P278-PCCA-PCCB
Propionic acidemia
P190-CHEK2
Susceptibility to breast cancer; Susceptibility to other cancer types
P319-Thyroid
Thyroid dysgenesis
P098-Wilson disease
Wilson disease
P102-HBB
Beta-thalassemia; Persistence of foetal haemoglobin, hereditary (HPFH); Sickle cell anaemia (SCA); Sickle cell disease (SCD)
ME011-MMR
Mismatch repair genes (MMR)
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