Conventional / global / constitutive KO
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Browse 2 Ndufs2 mouse models including conditional knockout, knockout variants from ingenious targeting laboratory. Available as Ndufs2 conditional knockout mouse, Ndufs2 knockout mouse. Contact us for availability and fast turnaround.
Encoding the mouse ortholog of human NDUFS2, Ndufs2 specifies the 49 kDa core subunit that, together with NDUFS7, NDUFS3 and ND1, builds the quinone-binding chamber of complex I, shaping the terminal N2 cluster environment and coupling quinone reduction to the conformational changes that drive proton translocation in the membrane arm. Biallelic human variants cause Leigh syndrome, hypertrophic cardiomyopathy and optic atrophy with isolated complex I deficiency, and structural work shows that Q-site mutations can uncouple electron transfer from pumping rather than simply reducing enzyme amount. That mechanism argues for patient missense knockins when the goal is to model partial, uncoupled activity, and for conditional nulls with cardiomyocyte, neuronal or retinal Cre when the question is tissue tolerance of complex I loss, since a germline null is not viable. No paralog substitutes for a core subunit. Choose endpoints separating coupling from capacity, including proton pumping and membrane potential, quinone site inhibitor sensitivity, respirometry, echocardiography, and retinal ganglion cell quantification.
ingenious targeting laboratory offers 2 distinct Ndufs2 (NDUFS2) catalog mouse models, featuring conditional knockout and standard 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 |
|---|---|
| 2 Ready Catalog Lines | Conditional Knockout (cKO) |
| Custom Model Generation | Constitutive Knockout (KO) |
| Advanced Modifications | Humanized, Knockin, Transgenic |
Knockout
Conditional knockout
Knockin
Humanized
Transgenic / overexpression
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Knockout, conditional, knockin, humanized, and related paths for Ndufs2 (human NDUFS2). Catalog lines ship when inventory exists. Everything else is a generation quote.
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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
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Specify rabbit on quote
Background substrain on quote
Background strain on quote
2 Ndufs2 lines with QC documentation and technical support. Ndufs2 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
We have 2 Ndufs2 models available — including Conditional Knockout, 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 Ndufs2 knockout mouse has the Ndufs2 gene permanently inactivated, enabling loss of function studies. A Ndufs2 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Ndufs2, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Ndufs2 organized by modification type. Each URL is indexable and matches common search patterns.