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Human EGFR Gene Mutation Detection Kit (Fluorescence PCR Method)
EGFR is the most common driving gene in Asian non small cell lung cancer (NSCLC) populations, with a mutation frequency of about 30% in NSCLC, about 50% in lung adenocarcinoma, and about 5% in lung squamous cell carcinoma. The EGFR gene has become an impo
This kit is used for in vitro qualitative detection of 31 somatic mutations in the EGFR gene extracted from peripheral blood (plasma or serum) samples of lung cancer patients. For advanced lung cancer patients, when it is not possible to obtain lung cancer tissue samples, peripheral blood samples can be selected for EGFR mutation gene detection; If pathological tissue can be obtained, it is recommended to prioritize the extraction of detection results from pathological tissue.
High sensitivity and sample saving: EGFR gene mutations with content as low as 0.1-0.5% can be detected in 10 ng DNA samples Comprehensive and comprehensive site guidance for drug use: capable of detecting 31 mutation sites, covering the sensitive and resistant sites of the first/second/third generation EGFR-TKIs It can be used for testing various types of specimens: fresh, frozen, and paraffin embedded tissues; Chest fluid, serum, plasma