
Uniform coverage for accurate CNV results.
High gene coverage for comprehensive CNV detection.
Six easy steps with minimal hands on time and direct-to-sequencer loading capability.
Our current panel range focuses on hereditary cancer markers, as well as hematological malignancies, including multiple myeloma and acute lymphoblastic leukemia. In addition to our current products, we are actively developing new digitalMLPA assays for a wide range of applications.
digitalMLPA is a PCR-based technique that enables the detection of up to 1200 targeted DNA sequences in a single multiplex reaction. After the PCR-based amplicon generation, each probe amplicon is quantified using an Illumina NGS platform. digitalMLPA does not require post-PCR clean up or library concentration measurements, making the technique efficient and user-friendly.
Coffalyser digitalMLPA™ is our free and easy-to-use data analysis software that makes analysing digitalMLPA experiments fast and effortless. Coffalyser digitalMLPA can automatically recognise digitalMLPA sequence reads from FASTQ files, and directly uses them for data analysis. Thanks to its advanced quality checks and algorithms, Coffalyser digitalMLPA can quickly detect and analyse aberrations in your samples, providing you with clear and detailed reports for every experiment.
SALSA® digitalMLPA™ products are for research use only (RUO). Not for use in diagnostic procedures.
Learn more: https://www.mrcholland.com/technology/digitalmlpa
General information: https://www.mrcholland.com/
D001 Hereditary Cancer Panel 1 detects copy number variations in 28 relevant oncogenes. CNVs in these genes are associated with a hereditary predisposition to a variety of cancer types including breast, ovarian, colorectal, gastric, prostate, pancreatic, endometrial, and melanoma.
D006 Multiple Myeloma detects copy number abnormalities on various chromosomal arms (1p, 1q, 13q, 17p) and in multiple-myeloma-associated genes. In addition, the panel detects trisomies, hyper- and hypodiploidy, and the BRAF V600E mutation associated with this malignancy.
D007 Acute Lymphoblastic Leukemia detects gains and losses in 73 specific target genes and 8 chromosomal regions (including 5q, iAMP21 and PAR1) associated with ALL. The panel can be used to examine intragenic copy number alterations, partial chromosome gains, losses and high-level amplifications, as well as gross ploidy changes and intrachromosomal gene fusions.
SALSA® digitalMLPA™ products are for research use only (RUO). Not for use in diagnostic procedures.
Learn more: https://www.mrcholland.com/technology/digitalmlpa
General information: https://www.mrcholland.com/
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