We build the exact model your study needs.

Designed and delivered by ingenious targeting laboratory. Quote in 24 hours.

Skip to main content

skin specific Cre mouse lines for conditional alleles

Conditional deletion of Target limits the genetic change to the lineage you choose. That helps in oncology, immunology, and metabolic work where systemic loss would muddy the read. After you confirm Cre specificity, crossing to Target floxed stock yields usable cohorts. For skin work, plan Cre specificity, reporter crosses, and baseline phenotyping before you scale.

Drivers used in skin programs

Conditional knockout focuses the experiment on skin while the rest of the animal keeps a wild type allele. That pattern mirrors somatic mutation in patients and avoids systemic compensation that can erase subtle phenotypes. It is often preferred when a germline null is lethal, weak, or confounded by developmental rescue. Knockin and humanized formats keep regulatory context at the endogenous locus. For skin focused programs, that matters when expression timing, splice isoforms, or allele dosage drive biology. Random integration transgenics can still help, but targeted alleles usually give cleaner pharmacology readouts.

  • K14-Cre

    Constitutive recombinase activity in the labeled lineage under this promoter system.

  • K14-CreERT2

    Inducible via tamoxifen control. Pair timing experiments with reporter crosses before scaling cohorts.

Popular floxed genes crossed to skin drivers

H2 conditional knockout (skin)Stk11 conditional knockout (skin)Cdkn2a conditional knockout (skin)Fbn1 conditional knockout (skin)Hbb conditional knockout (skin)Nipbl conditional knockout (skin)

Frequently asked questions

What does skin specific Cre mean?

skin specific Cre drivers recombine floxed alleles primarily in that lineage. Practical work still demands reporter crosses to verify efficiency in your facility because genetic background and copy number nudge leak profiles.

Should I use inducible CreERT2 for skin studies?

Inducible systems help when developmental deletion confounds adult phenotypes or when you need tight timing around injury or tumor onset. Tamoxifen protocols carry their own controls, which we document in project planning.

Where do I find floxed models to pair with these drivers?

Our catalog lists floxed conditional lines by gene. If your favorite target is not listed, we quote generated flox builds and crossing plans so you reach cohort size on a clear schedule.

References

Request a quote