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Lineage Tracing Mouse Models

Since 1998, ingenious targeting laboratory has engineered over 125 lineage tracing models including inducible Cre-dependent reporters, multi-color switching systems, and tissue specific fate mapping approaches, contributing to 103+ peer reviewed publications in cell fate determination and lineage diversity studies. Lineage tracing answers fundamental developmental and regenerative biology questions: Where do cells originate? What descendants do they produce? When do cell fate decisions occur? Which signals govern lineage commitment? These questions require sophisticated reporter systems revealing cell history.

2,500+
Projects Completed
800+
Publications
26+
Years Experience
100%
Success Rate

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Our scientific consultants are ready to discuss your research requirements and recommend the optimal approach for your program. Initial consultation is provided at no charge.

✦ New for 2026

Breeding Scheme Architect

Plan complex multi-allele breeding strategies, calculate expected genotype ratios, and estimate time to experimental cohorts—all before starting your project.

Visualize multi-generation breeding paths
Calculate Mendelian ratios automatically
Estimate timeline to study-ready cohorts

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Allele 1Gene-flox (conditional)
Allele 2Cre-driver (tissue-specific)
TargetHomozygous knockout

→ 3 generations to target genotype

Frequently asked questions

Common lineage tracing reporters include Rosa26-tdTomato (red fluorescent protein), Rosa26-GFP (green fluorescent protein), Rosa26-LacZ (beta-galactosidase), and multi-color systems like Rosa26-Confetti (stochastic color switching). Selection depends on imaging modality, tissue type, and whether multi-color clonal analysis is needed.

Tamoxifen-inducible Cre (CreER) provides temporal control of reporter activation. A single tamoxifen pulse marks cells expressing the Cre driver at that moment. All descendants of those marked cells retain the reporter, enabling tracking of cell fate decisions and clonal expansion over time.

Yes. Lineage tracing and conditional knockout can be combined by crossing a CreER driver to both a reporter line and a floxed target gene. Tamoxifen treatment simultaneously marks cells (lineage tracing) and deletes the target gene (conditional knockout), enabling study of gene function specifically in traced cell populations.

Common CreER drivers include tissue specific promoters (e.g., Myh6-CreER for cardiomyocytes, Albumin-CreER for hepatocytes, Nestin-CreER for neural cells) and cell type specific promoters (e.g., alpha-SMA-CreER for smooth muscle, CD4-CreER for T cells). Selection depends on the cell population you want to trace.

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Discover reporter systems, Cre drivers, and cell fate mapping strategies from expert PhD scientists.

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