Overview

Charles River offers potent, inducible, and reversible RNAi-mediated gene silencing for your gene of interest in mouse models. Our state-of-the-art microinjection services transform custom ES cells into your in vivo research model in about 12 weeks.

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Advantages

RNAi-mediated gene silencing puts the power of complex genetic modifications within reach more quickly and efficiently than traditional knockout technologies or intercross methods.

  • Inducible and reversible nature of gene suppression allows essential function or embryonic lethal genes to be manipulated in vivo.
  • Suppressing gene function better mimics the activity of small-molecule agonists compared to knocking out the gene.
  • Controlling the timing and duration of gene suppression allows increased flexibility in experimental design.

Timeline for RNAi Production

Estimated time: 24-30 weeks

  • Project initiation
  • Three-month mark: Generation of potent shRNAs
  • Five-month mark: Generation and validation of target RNAi ES cell lines
  • Six-month mark: Generation of ES cell-derived RNAi mice

Please note: This service is available through North America only.