New libraries. New capabilities. New discoveries.

Thermo Fisher Scientific is applying the power of the CRISPR-Cas9 system to high throughput screening applications with our new awarding winning Invitrogen™ LentiArray™ CRISPR libraries. These arrayed CRISPR libraries are designed to provide you with a flexible system that adapts to your needs and your screening goals. 

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Advance your research with award-winning solutions

LentiArray™ CRISPR Libraries made The Scientist’s Top 10 Innovations of 2016!

“The LentiArray CRISPR libraries have allowed us to make significant inroads in our research on pediatric cancer, discovering a potentially novel strategy for the treatment of deadly brain tumors,” said Simone Treiger Sredni M.D., Ph.D., associate professor of pediatric neurosurgery at Northwestern University Feinberg School of Medicine. “Through the use of lenti-viral CRISPR-Cas9 particles, we identified an enzyme that can be inhibited by drugs and has been shown to prohibit tumor cell growth without affecting normal cells.”

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LentiPool CRISPR libraries

LentiPool™ CRISPR libraries are an affordable method to screen a large number of genes, as there is no high-throughput instrumentation required.  Request for more information.

The CRISPR-Cas9 system provides an efficient method for specific, complete, and permanent gene knockout and is a potent tool for making new discoveries about gene function. The LentiArray CRISPR library collections harness this capability and expand it into high throughput applications to create the next generation of tools for functional genomics screening. 

Features of the LentiArray Libraries

  • Arrayed libraries in flexible formats to allow for a wide array of assays
  • Advanced gRNA designs for maximum knockout efficiency without sacrificing specificity
  • Up to 4 high quality gRNAs per gene target for efficient knockout in a wide variety of cell types
  • Complete set of controls to streamline assay development
  • 19 defined libraries and custom options available allowing you to focus on defined gene sets or perform unbiased whole genome surveys.
  • Single gRNA and custom arrays available to support rapid validation of hits