| Products/Services Used | Details | Operation |
|---|---|---|
| Gene Fragments> | The dsDNA fragment containing ltDHFR(DD)-CreERT2, flanked by EcoRI and NotI sites, was synthesized by GenScript Biotech and used to replace CreERT2 in the fabp10a:CreERT2; cryaa:mCerulean construct 61 using restriction enzyme-based cloning with EcoRI/PacI followed by ligation with T4 ligase. To generate the fabp10a:lox2272-loxp-nls-mTagBFP2-stop-lox2272-H2B-mGL-stop-loxpmCherry-NTR2; cryaa:mCherry construct [abbreviated as fabp10a:BB-NTR2], the dsDNA sequence of BB-NTR2 flanked with EcoRI/PacI was synthesized by GenScript Biotech and used to replace BB-NTR in the fabp10a:BB-NTR; | Get A Quote |
Regeneration can rely on multiple cellular sources, including stem cells, self-duplicating cells, and transdifferentiating cells. A central question in regenerative biology is how these distinct lineages contribute to repair and interact within a functionally regenerated tissue. We previously developed the CellCousin system to study cellular plasticity using inducible recombination and nitroreductase-mediated ablation in zebrafish. Here, we present CellCousin2, which introduces two key improvements for the long-term tracking of spared and regenerating cells. First, to reduce background recombination, we developed a Dihydrofolate Reductase (DHFR)-CreER system with dual control: DHFR-mediated degradation in the a... More