The development of efficient and reliable ways to make precise, targeted changes to the genome of living cells is a long-standing goal for biomedical researchers. Recently, a new tool based on a bacterial CRISPR-associated protein-9 nuclease (Cas9) from the bacteria Streptococcus pyogenes has induced considerable excitement both as a research tool and for its possible commercial utilizations.
The possibilities for this new tool is enormous and this new technology/tool is set to become a patent battleground as companies has started to position themselves over who will control the tool and its products. There are 3 major players who are currently trying to gain control over the IPR position and it will be interesting to follow the process.
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