Artemis

SERVICES . ARTEMICE® CONDITIONAL®

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This section describes the work flow for the generation of ArteMice® CONDITIONAL® custom made mice. Terms and conditions for these services are available on request.

  1. Conditional KO to produce floxed heterozygous mice
    Deliverable: 2 breeding pairs of floxed heterozygous mice
    Time: 40 Weeks

    • Locus characterization
    • Conditional KO Vector construction
    • Transfection of vector into C57BL/6 ES cells
    • ES Cell injection
    • In vivo selection marker deletion (parallel with germline transmission)
    • Breeding to heterozygosity

      Upon request, optional breeding to homozygosity with an ArteMice® Recombinase Zoo mouse.

      Deliverable: 2 breeding pairs of homozygous mice with cre
      Time: 66 Weeks


  2. Conditional KO to produce C57BL/6 homozygous mice containing CreER gene switch
    Deliverable: 2 breeding pairs of homozygous mice with CreER gene switch
    Time: 52 Weeks

    • Locus characterization
    • Conditional KO Vector construction
      Transfection of vector into C57BL/6 ES cells, containing CreER gene switch
    • ES Cell injection
    • In vivo selection marker deletion (parallel with germline transmission)
    • Breeding to homozygosity

  3. Conditional KO to produce F1 homozygous mice containing CreER gene switch
    Deliverable: three male and female homozygous F1 ES mice
    Time: 44 weeks

    • Locus characterization of C57BL/6 and 129 alleles
    • Conditional KO Vector construction for both alleles
    • Consecutive transfection into F1 ES Cells containing CreER to target both alleles
    • In vitro deletion of selection markers
    • Selection of male and female homozygous ES Cells
    • ES Cell injection of male and female homozygous ES Cells

  4. Conditional KO to produce F1 heterozygous mice containing CreER gene switch
    Deliverable: five male heterozygous ES mice
    Time: 36 weeks

    • Locus characterization of C57BL/6 allele
    • Conditional KO Vector construction for one alleles
    • Transfection into F1 ES Cells containing CreER to target one alleles
    • In vitro deletion of selection marker
    • ES Cell injection of male heterozygous ES Cells
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