LUNG ADENOCARCINOMA: SANGER SEQUENCING OF THE BRAF GENE

LabGenetics
Caja de LUNG ADENOCARCINOMA: SANGER SEQUENCING OF THE BRAF GENE

Delivery time

4-6 weeks

Sample

Biopsy tissue

900,00€
Caja de LUNG ADENOCARCINOMA: SANGER SEQUENCING OF THE BRAF GENE

BRAF gene analysis using Sanger sequencing allows for the identification of somatic mutations associated with lung adenocarcinoma, particularly the V600E mutation, which abnormally activates the MAPK/ERK pathway, promoting cell proliferation. This study has significant clinical relevance, as the detection of BRAF mutations guides targeted therapies with BRAF and MEK inhibitors, personalizing treatment and improving prognosis. Furthermore, this analysis is crucial in tumors that are negative for EGFR, ALK, or ROS1, within the comprehensive diagnostic approach for non-small cell lung cancer.

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Custom sequencing panels (1 to 15 genes)

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