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Innovation To Be The Progressive Factor For Prime Editing Market

Prime editing is the gene-editing method that can insert, delete and do base swapping accurately. Prime editing also termed as ‘genetic word processor’ precisely select the target DNA and replace genetic code.

Targeting 75,000 different mutations and correcting 89% of genetic defects will drive the demand for prime editing. In 2017, the first gene editing in the human body was attempted. Gene editing in a patient with Hunter’s syndrome was tested for safety and concluded reliable shreds of evidence.

Superior target flexibility and editing precision with minimal errors make Prime editing first preference over the other conventional technique such as CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats). Application of prime editing in reversing Genetic disease will be a milestone in gene editing.

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Increasing prevalence of genetic disease creates a huge opportunity for prime editing market. Successful preliminary results with a genetic disease like Tay Sachs and Sickle cell anaemia will drive the prime editing market.

Technological advancements providing minimal error with this technique will fuel the growth of prime editing. Decreased cost of DNA sequencing will propel prime editing market for research and commercialization.

Arising ethical and safety concerns will make prime editing highly regulated sector. This may limit the scope and can restraint the growing market. Detrimental effect on Genetic diversity due to genetic engineering in one way may limit the market scope.

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Market Segmentation

Based on application
  • Genome editing
  • Genome regulation
  • Gene edited cell therapies
  • Cell line engineering
Based on end user
  • Biotechnology Companies
  • Academic Institutions
  • Government Laboratories
  • Contract Research Organizations

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Examples of some of the market participants in Prime Editing market identified across the value chain Beam Therapeutics Inc., Precision BioSciences, Inscripta, Inc, Horizon Discovery Ltd., Sangamo Therapeutics, Inc., CRISPR Therapeutics., Intellia Therapeutics, Inc., and others.

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