Conventional / global / constitutive KO
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Browse 2 Fgf13 mouse models including conditional knockout, knockout variants from ingenious targeting laboratory. Available as Fgf13 conditional knockout mouse, Fgf13 knockout mouse. Contact us for availability and fast turnaround.
Fgf13, mouse ortholog of human FGF13, encodes an intracellular FGF homologous factor whose multiple N-terminal splice isoforms are generated from an X-linked locus and which acts through two distinct nonreceptor mechanisms: docking on the C-terminal tails of voltage-gated sodium channels including NaV1.6 to control inactivation and availability, and direct microtubule binding that stabilizes polymers during neuronal polarization and axon branching. It is also a thermal nociception regulator in sensory neurons and contributes to cardiomyocyte excitability. Human hemizygous loss-of-function variants cause X-linked intellectual disability with epilepsy and febrile seizure susceptibility, which makes patient-derived truncating or missense knockins, together with isoform-specific targeting, more informative than whole-gene deletion. Nulls are viable, permitting conditional floxed alleles with Nestin-Cre, Advillin-Cre, or Myh6-Cre to separate cortical, sensory, and cardiac contributions, and X-linkage requires careful hemizygous versus mosaic female design. Paralogs Fgf11, Fgf12, and Fgf14 share channel partners, so compound alleles clarify which factor sets the excitability endpoint being measured.
ingenious targeting laboratory offers 2 distinct Fgf13 (FGF13) catalog mouse models in the FGF family, 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 Fgf13 (human FGF13). 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 Fgf13 lines with QC documentation and technical support. Fgf13 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
We have 2 Fgf13 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 Fgf13 knockout mouse has the Fgf13 gene permanently inactivated, enabling loss of function studies. A Fgf13 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Fgf13, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Fgf13 organized by modification type. Each URL is indexable and matches common search patterns.