Sanger sequencing is a powerful and accurate method for deciphering the genetic code, widely used to map the sequence of nucleotides in DNA. This technique, developed by Frederick Sanger, has been essential in advancing genetic research, disease diagnostics, and biotechnology. Despite the rise of newer technologies, Sanger sequencing remains a go-to method for precise, high-quality genetic analysis in both research and clinical applications.
https://eurofinsgenomics1....

Amplifying Detection: LNA Probe Applications
This initiative investigates the diverse applications of Locked Nucleic Acid (LNA) probes in molecular biology. LNA probes, distinguished by their enhanced stability and sensitivity, offer promising avenues for improving detection in various research, diagnostic, and therapeutic contexts. By leveraging the unique characteristics of LNA, including heightened affinity and specificity, researchers aim to refine nucleic acid detection assays for increased accuracy and efficiency.
https://eurofinsgenomics.c...