Conventional / global / constitutive KO
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Browse 1 Ndufa12 mouse model including conditional knockout variants from ingenious targeting laboratory. Contact us for availability and fast turnaround.
Final maturation of complex I depends on Ndufa12, the mouse ortholog of human NDUFA12, which encodes the B17.2 subunit added late to the N module of complex I, capping the peripheral arm once the FMN and iron-sulfur chain are in place, and it must be distinguished from its paralogous assembly chaperone NDUFAF2, formerly B17.2L, which transiently occupies the same site during biogenesis. Human NDUFA12 loss causes Leigh syndrome and optic atrophy with isolated complex I deficiency, and cells lacking it retain a nearly complete but functionally impaired enzyme, indicating a role in the terminal capping step and in stabilizing electron flow toward quinone. This makes a null allele genuinely informative, since the resulting phenotype is a misfinished rather than absent complex, while patient knockins allow allele-specific severity comparisons. The NDUFAF2 relationship is the real caution here, since retained chaperone occupancy can blunt phenotypes. Align allele with endpoints including in-gel activity, NDUFAF2 retention assays, retinal ganglion cell counts, and brainstem lesion progression.
ingenious targeting laboratory offers 1 distinct Ndufa12 (NDUFA12) 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
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Knockout, conditional, knockin, humanized, and related paths for Ndufa12 (human NDUFA12). 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 Ndufa12 line with QC documentation and technical support. Ndufa12 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
Ndufa12-Flox
CKOCKO
These mice carry loxP sites flanking exon2 of Ndufa12 gene. When crossed with a Cre recombinase-expressing strain, this strain is useful in eliminating tissue-specific conditional expression of Ndufa12 gene.
We have 1 Ndufa12 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.
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Order catalog modelA Ndufa12 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Ndufa12, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Ndufa12 organized by modification type. Each URL is indexable and matches common search patterns.
Send the Ndufa12 line to a U.S. barrier facility for colony maintenance, cohort production, and complex breeding schemes through mouse breeding services.