Lung Cancer Panel NGS library preparation Kit

Lung Cancer Panel NGS library preparation Kit

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.

Lung cancer is one of the lead causes of cancer death in the United States and worldwide. The two main types of lung cancer are small-cell lung carcinoma (SCLC) and non-small-cell lung carcinoma (NSCLC). Atila Lung Cancer Panel NGS library preparation Kit targets 138 amplicon regions of 24 lung cancer related genes, including AKT1, ALK, BAP1, BRAF, CCDC6, EGFR, EML4, ERBB2, FGFR2, KDR, KRAS, LRIG3, MAP2K1, MAP2K2, MYCL1, NFE2L2, RB1, RET, ROS1, SLC34A2, SMARCA4, STK11, TFG, 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.

Features

• High sensitivity: The kit can use as low as 100pg purified DNA
• Short preparation time: Sample library is ready within 2.5-3 hours.
• Simple procedures: Hands-on time is as short as 30 minutes.
• High specificity: high on target rate and high uniformity.

*  This products is for research use only in US