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Encyclopedia of Experiments

CreER-LoxP System-Based Target Gene Inactivation: A Tamoxifen-Inducible Cre Recombinase System for Target Gene Knockout in a Mouse Model

Overview

This video describes a procedure for target gene knockout using a tamoxifen-inducible Cre-recombinase system following intraperitoneal injection of tamoxifen in a mouse model.

Protocol

All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.

1. Induction of Transfected CreER with Tamoxifen

CAUTION: Tamoxifen is harmful, may be cancerous or damage fertility. Please refer to the safety data sheet.

  1. Plan intraperitoneal tamoxifen injections on three consecutive days.
  2. On day 1, dissolve 10 mg of tamoxifen in 40 µL ethanol. Incubate at 55 °C for 10 min. Vortex several times until the tamoxifen has dissolved.
  3. Add 960 µL corn oil. Incubate for 5 mins at 55 °C. Vortex several times to get a clear solution.
  4. Prepare the solution in a 1-mL insulin syringe with a 27 G needle.
  5. Scruff the mouse by grabbing the neck of the mouse carefully with the thumb and the second finger, fixing the tail between the base of the hand and the fourth and fifth finger.
  6. Inject 0.1 mL (= 1 mg of tamoxifen) of the solution intraperitoneally into the left lower quadrant of the abdomen.
  7. Repeat the injections on days two and three.

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Materials

Name Company Catalog Number Comments
Injekt Syringe F 1 ml  Braun  9166017V  For intraperitoneal injection
Tamoxifen  Sigma-Aldrich T5648-1G  For CreER activation
Corn oil  Sigma-Aldrich C8267-500ML  Carrier for tamoxifen injections

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