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Genome Editing
AcceGen offers comprehensive genome editing services for cell lines, catering to various research endeavors. Our streamlined protocols ensure efficient gene knock-out in standard cell lines, while customized approaches are developed for complex projects like knock-in, point mutations, and tagging.
We provide end-to-end solutions, from project design to cell characterization, utilizing diverse techniques such as plasmid-based approaches and Cas9 protein delivery to achieve precise genome modifications.
Figure 1. CRISPR/Cas9 enables targeted DNA modifications in organisms.
Our services include:
- Gene Overexpress
- RNA Interference
- CRIPSR/Cas9
Our team of experts is experienced in successfully executing genome editing projects, coupled with a strong commitment to maintaining rigorous quality control measures. Through sequencing and Western blot analysis, we accurately characterize editing events and ensure precise outcomes. With our comprehensive genome editing services, researchers can confidently advance their studies and gain valuable insights into cellular functions and mechanisms. With AcceGen as your trusted partner, you can embark on your research journey with confidence, knowing that accurate and reliable results are within reach.
Our services include:
- Disease Modeling: Introducing mutations for studying disease mechanisms, testing therapies, and identifying drug targets.
- Functional Genomics: Modifying genes to uncover their functions and interactions, providing insights into biological processes.
- Gene Therapy: Targeted modification of disease-causing mutations in patient cells to cure genetic disorders at their root cause.
