Conventional / global / constitutive KO
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Browse 1 Cox7b mouse model including conditional knockout variants from ingenious targeting laboratory. Contact us for availability and fast turnaround.
Cox7b, the mouse ortholog of human COX7B, encodes a small nuclear encoded transmembrane subunit of cytochrome c oxidase incorporated into the late assembly module that completes the shell surrounding the catalytic core, and the gene is X-linked in both species. Human COX7B mutations cause microphthalmia with linear skin defects, an X-linked dominant disorder with male lethality in which skewed X inactivation in females produces mosaic complex IV deficiency, biology that makes X-linked mosaicism itself the experimental variable. Design therefore differs from autosomal COX genes: heterozygous females model mosaic deficiency and developmental patterning defects, while conditional deletion in males tests absolute tissue requirement without whole embryo loss. No paralog substitutes for 7B in somatic tissues. Use Rosa26-CreER, Nes-Cre, or Krt14-Cre depending on whether skin, eye, or nervous system is the endpoint, then read COX histochemistry, clonal patch analysis, complex IV activity, and blue native assembly profiles.
ingenious targeting laboratory offers 1 distinct Cox7b (COX7B) catalog mouse model, featuring conditional knockout. Researchers can order pre-developed catalog lines or request a custom mouse model, including humanized, knockin, and transgenic variations with verified germline transmission.
| Model Availability | Allele Class Options |
|---|---|
| 1 Ready Catalog Line | Conditional Knockout (cKO) |
| Custom Model Generation | Constitutive Knockout (KO) on request |
| Advanced Modifications | Humanized, Knockin, Transgenic |
Knockout
Conditional knockout
Knockin
Humanized
Transgenic / overexpression
Prefer the order form? Order. Need an allele that is not listed? Request a quote.
Knockout, conditional, knockin, humanized, and related paths for Cox7b (human COX7B). Catalog lines ship when inventory exists. Everything else is a generation quote.
Specify tissue or Cre driver on quote
Convertible floxed allele pathway
Multi allele / compound knockout project
BAC scale deletion or targeting
LSL or conditional expression knockin
Domain or partial humanization scope
Checkpoint IO humanization when gene is a checkpoint target
Multi humanized / combination IO project
BAC transgenic or large fragment insert
Tamoxifen or dox inducible Cre
Dual recombinase breeding scheme
Flp or FRT derivative allele pairing
Catalog reporter lines not tied to a single gene allele
Specify rat on quote
Specify rabbit on quote
Background substrain on quote
Background strain on quote
1 Cox7b line with QC documentation and technical support. Cox7b floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
Cox7b-Flox
CKOCKO
These mice carry loxP sites flanking exon2 of Cox7b gene. When crossed with a Cre recombinase-expressing strain, this strain is useful in eliminating tissue-specific conditional expression of Cox7b gene.
We have 1 Cox7b model available — including Conditional Knockout types. Contact us today for current availability and our fastest turnaround options. All models come with full QC documentation and technical support.
Best pricing in the industry. Get a quote in 24 hours. Our team of PhD scientists is available to help you select the right model for your research.
Order catalog modelA Cox7b conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Cox7b, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Cox7b organized by modification type. Each URL is indexable and matches common search patterns.
Send the Cox7b line to a U.S. barrier facility for colony maintenance, cohort production, and complex breeding schemes through mouse breeding services.