Ttr-CreERT2
Product ID:
C001767
Background:
C57BL/6JCya
Documents:
Expressing Tissues/Cells:
Liver, choroid plexus, retinal pigment epithelial cells, hippocampus, pancreas, and Ttr-positive cells
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Strain Description
Ttr-CreERT2 mice are generated via genome editing by replacing the TGA stop codon of the mouse Ttr gene with a P2A-CreERT2 cassette. Without tamoxifen treatment, CreERT2 recombinase primarily resides in the cytoplasm; nuclear translocation and recombination activity of CreERT2 only occur upon tamoxifen stimulation. When crossed with mice containing loxP sites, offspring are expected to undergo Cre-mediated recombination between loxP sites specifically in Ttr-positive cells following tamoxifen administration.
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