Colorectal Cancer Panel Sequencing Library Preparation Kit
This kit targets amplicon regions of cancer related genes and provides superior sensitivity for detection of cancer mutations. The resulting sample library is compatible with Illumina NGS sequencing.
Each kit includes 100 reactions.
This product is for research use only.
Colorectal Cancer Panel Sequencing Library Preparation Kit
The Atila Colorectal Cancer Panel Sequencing Library Preparation Kit targets amplicon regions of 21 Colorectal cancer related genes, including AKT1, APC, AXIN1, BRAF, CTNNB1, EP300, FBXW7, KRAS, MAP2K1, MAP2K4, MDM2, MLH1, MSH2, MSH6, MUTYH, PIK3CA, PIK3R1, PMS1, PMS2, TCF7L2, and TP53 etc. The resulting sample library is compatible with Illumina NGS sequencing.
The current method employs novel primer design strategies, greatly simplifies sample preparation procedures, and enables rapid screening and discovering genetic variations.
Colorectal cancer is a cancer that starts in the colon or the rectum. The American Cancer Society estimate that about 4.8% men and 4.3% women in the United States will develop colorectal cancer during their lifetime. It is one of the most leading causes of cancer death worldwide.
Cancer is a type of diseases caused by accumulation of genetic changes, which results in abnormal cell growth and invasive behaviors that potentially spread to other body parts. Most common nucleotide sequence changes in cancer involve single-nucleotide variants and small insertions or deletions.
Features Include
Technical Specs
Workflow Overview for the Colorectal Cancer Panel Sequencing Library Preparation Kit
This section is for demonstrative purposes only and may be incomplete or inaccurate. Always refer to the product instructions for precise guidelines and directions.
Illumina sequencing.
