Conventional / global / constitutive KO
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Browse 2 Ndufb8 mouse models including conditional knockout, knockout variants from ingenious targeting laboratory. Available as Ndufb8 conditional knockout mouse, Ndufb8 knockout mouse. Contact us for availability and fast turnaround.
Ndufb8, ortholog of human NDUFB8, encodes the ASHI subunit of complex I, a membrane arm accessory protein of the distal ND module whose abundance is unusually informative experimentally, since NDUFB8 immunolabeling paired with SDHA forms the standard quadruple immunofluorescence readout used to detect complex I deficiency in patient and mouse tissue at single-cell resolution. Biallelic human variants cause complex I deficiency with Leigh-like encephalopathy, and loss destabilizes the holoenzyme while subassemblies persist. This dual role as structural subunit and diagnostic marker has a practical consequence: any allele that removes or alters the epitope invalidates the very assay commonly used to phenotype it, so tagged or humanized knockins must be designed with antibody epitopes deliberately preserved or matched. A conditional null with neuronal or muscle Cre remains the tool for threshold mapping. Align allele with endpoints including quadruple immunofluorescence, BN-PAGE with in-gel activity, respirometry, and neuropathological lesion scoring.
ingenious targeting laboratory offers 2 distinct Ndufb8 (NDUFB8) 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 Ndufb8 (human NDUFB8). 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
2 Ndufb8 lines with QC documentation and technical support. Ndufb8 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
We have 2 Ndufb8 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 Ndufb8 knockout mouse has the Ndufb8 gene permanently inactivated, enabling loss of function studies. A Ndufb8 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Ndufb8, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Ndufb8 organized by modification type. Each URL is indexable and matches common search patterns.