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Simultaneously detect 28 common mutations in 4 genes in three stool samples within 48 hours
Colorectal Cancer, or Bowel Cancer, is the second largest cause of cancer mortality in the Western world. However, it is also among the most curable cancers when detected early. With regular screening from 50 years, pre-cancerous lesions and polyps can be detected and removed before they can become cancerous. This highlights the importance of colorectal cancer screening for early detection.
Stool DNA (sDNA) screening offers a non-invasive yet highly specific screening method to identify high risk individuals that would benefit from a colonoscopy. The Ranplex CRC Array tests colorectal cells that have been shed into the stool, for 28 mutations that are common in colorectal cancer and pre-cancerous growths. The screening test is performed on a single stool sample, without the need for any patient preparation.
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