Numelab | News

Detecting hundreds of the most commonly mutated genes involved in cancer

Molecular Diagnostics / Cell Biology / Molecular Biology

January 23, 2017

How can you survey more than 100 oncogenes and tumor suppressor genes in your cancersamples?

The newly developed Human Comprehensive Cancer Panel allows you to enrich genes and construct libraries for NGS analysis of hundreds of genes most commonly mutated in cancer, covering oncogenes, tumor suppressor genes, genes involved in angiogenesis, apoptosis, DNA damage and repair, epigenetics, immune responses, etc. The system provides you with a complete Sample to Insight solution and a simple, streamlined workflow for routine known and novel cancer mutation detection on any NGS platform from Illumina and Ion Torrent.

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Simple new prenatal blood test for early and accurate detection of major chromosomal abnormalities

Molecular Diagnostics / Cell Biology / Molecular B...

Multiplicom is proud to launch Clarigo™, a new CE-IVD1 non-invasive prenatal test (NIPT). This highly accurate blood test will enable genetic analysis laboratories to detect the presence or absence of major chromosomal abnormalities such as trisomy 21 (Down’s syndrome), 18 (Edwards’ syndrome) and 13 (Patau syndrome), in the fetus, as early as in the first trimester of pregnancy by analysis of the fetus’s DNA in the maternal blood.

October 22, 2015 More +

IDEXX Colilert-18/Quanti-Tray Test Becomes the New ISO Standard 9308-2:2012

Molecular Diagnostics / Cell Biology / Molecular B...

IDEXX announces that its Colilert®-18/Quanti-Tray® test becomes the new International Organization for Standardization (ISO) worldwide standard for detecting total coliforms and E. coli in water. The Organization has withdrawn ISO 9308-2:1990, which follows the multiple tube (most probable number) method, and replaced it with ISO 9308-2:2012 using the Colilert-18/Quanti-Tray method.

August 01, 2013 More +