Conventional / global / constitutive KO
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Browse 1 Cacnb4 mouse model including conditional knockout variants from ingenious targeting laboratory. Contact us for availability and fast turnaround.
CaVβ4, encoded by Cacnb4 as the ortholog of human CACNB4, is the cerebellum-enriched β subunit that partners CaV2.1 at parallel and climbing fiber terminals, engaging the α-interaction domain through its guanylate kinase domain to control surface expression and inactivation kinetics; a short nuclear isoform additionally binds chromatin regulators and the phosphatase regulatory subunit B56δ, giving the gene a transcriptional arm independent of conductance. The spontaneous lethargic allele, a splice mutation that abolishes α1 binding, causes ataxia, absence-like spike-wave discharges and lymphocyte defects, and human variants segregate with juvenile myoclonic epilepsy and episodic ataxia. Because homozygous loss produces severe ataxia and seizures with poor postweaning survival, a conditional null crossed to Pcp2-Cre or a granule cell driver is the practical route to adult cerebellar physiology, while a patient missense knockin separates trafficking from nuclear signaling. Cacnb1, Cacnb2 and Cacnb3 partially substitute, so quantify β subunit stoichiometry directly.
ingenious targeting laboratory offers 1 distinct Cacnb4 (CACNB4) 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 Cacnb4 (human CACNB4). 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
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Specify rabbit on quote
Background substrain on quote
Background strain on quote
1 Cacnb4 line with QC documentation and technical support. Cacnb4 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
Cacnb4-Flox
CKOCKO
These mice carry loxP sites flanking exon4 of Cacnb4 gene. When crossed with a Cre recombinase-expressing strain, this strain is useful in eliminating tissue-specific conditional expression of Cacnb4 gene.
We have 1 Cacnb4 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 Cacnb4 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Cacnb4, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Cacnb4 organized by modification type. Each URL is indexable and matches common search patterns.
Send the Cacnb4 line to a U.S. barrier facility for colony maintenance, cohort production, and complex breeding schemes through mouse breeding services.