Achieving efficient delivery and editing
CRISPR-Cas9 is proving to be an efficient and customizable alternative to other existing genome editing tools. Since the CRISPR-Cas9 system itself is capable of cutting DNA strands, CRISPRs do not need to be paired with separate cleaving enzymes as other tools do. They can also easily be matched with tailor-made “guide” RNA (gRNA) sequences designed to lead them to their DNA targets. Tens of thousands of such gRNA sequences have already been created and are available to the research community. CRISPR-Cas9 can also be used to target multiple genes simultaneously, which is another advantage that sets it apart from other gene-editing tools
Related Conference of Achieving efficient delivery and editing
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21th World Congress on Tissue Engineering Regenerative Medicine and Stem Cell Research
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Achieving efficient delivery and editing Conference Speakers
Recommended Sessions
- Achieving efficient delivery and editing
- Cancer and stem cells
- CRISPR technologies and society
- CRISPR technologies beyond genome editing and gene regulation
- Genome editing and gene regulation in human health
- Genome editing and gene regulation in industrial bacterial biotechnology
- Genome editing and gene regulation in industrial eukaryotic biotechnology
- Genome Editing Methods and Novel Tools
- Horizons of CRISPR biology
- Plant and Animal Biotechnology
- Structural Biology and Bioinformatics
- Therapeutic Genome Editing
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