CRISPR and CAS Gene Market Growing Automation in Healthcare to Benefit Growth of the Market.




Clustered regularly interspaced short palindromic repeats (CRISPR) technology is a simple yet powerful nucleic acid-targeting editing tool for genome. It allows researchers to easily alter DNA sequences and modify gene function. It has potential applications, which include correcting genetic defects, treating, and preventing the spread of diseases. The technology is faster, cheaper, and more accurate than previous techniques of editing DNA such as ZFNs (Zinc Finger Nucleases) and TALENs (Transcription Activator-Like Effector Nucleases). Researchers are focusing on its use in animal models or isolated human cells, with the aim to eventually use the technology for routinely treating diseases in humans.


Furthermore, competition among the existing players has increased owing to technological developments and their potential applications. There has been an increased focus on the highly adaptable CRISPR technology. For instance, as of May 2020, Merck KGaA has received a total of 26 CRISPR patents worldwide. This indicates the increasing focus of biotechnology companies on CRISPR/Cas gene technology.


The CRISPR and Cas gene-based genome editing applications are more or less in a nascent stage of development and a considerable number of possible usages are still unchartered. These areas can later be a source of the significant untapped potential provided that specific product-based commercialization picks up the pace that numerous investors in the market are anticipating.


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