Conventional / global / constitutive KO
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Browse 6 Gba mouse models including conditional knockout, knockin, knockout variants — in stock and ready to ship from ingenious targeting laboratory. Available as Gba conditional knockout mouse, Gba knockin mouse, Gba knockout mouse. Request a quote within 24 hours.
Gba, the mouse ortholog of human GBA1, encodes lysosomal acid beta-glucocerebrosidase, a retaining glycosidase that cleaves glucosylceramide into ceramide and glucose, depends on saposin C for activity, and reaches the lysosome via LIMP2 (Scarb2) rather than the mannose-6-phosphate route. Biallelic loss causes Gaucher disease with glucosylsphingosine accumulation, whereas single variant alleles such as N370S and L444P are the strongest common genetic risk factors for Parkinson disease, acting through impaired lysosomal flux and a reciprocal loop between reduced enzyme activity and alpha-synuclein aggregation. Constitutive nulls die within a day of birth from a defective epidermal permeability barrier, so conditional deletion with nestin-Cre or microglial drivers is required for adult neuropathology, while point knockins preserve residual activity and model heterozygous risk. The non-lysosomal paralog Gba2 hydrolyzes the same substrate elsewhere, so interpret lipid panels accordingly and match allele class to storage, chaperone response, or synucleinopathy endpoints.
ingenious targeting laboratory offers 6 distinct Gba (GBA) catalog mouse models, featuring conditional knockout, standard knockout, and knockin. 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 |
|---|---|
| 6 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 Gba (human GBA). 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
6 Gba lines with QC documentation and technical support. Gba floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
Gba-Flox(2)
Conditional KnockoutKO/CKO mice
Gba-Flox
Conditional KnockoutKO/CKO mice, disease model mice
Gba-L401R
Knockinpoint mutantion mice
Gba-L462P
Knockinpoint mutantion mice
Gba-D427V
Knockinpoint mutantion mice
Gba-KO
KnockoutKO/CKO mice
Peer reviewed work involving Gba (GBA) from ITL supported projects.
We have 6 Gba models in stock — including Conditional Knockout, Knockin, Knockout types. In stock and ready to ship this week. All models come with full QC documentation, health certificates, and dedicated 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 Gba knockout mouse has the Gba gene permanently inactivated, enabling loss of function studies. A Gba conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Gba, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints. Gba knockin models carry a precisely inserted sequence at the Gba locus, useful for reporter, tag, or humanization studies.
Jump to catalog backed pages for Gba organized by modification type. Each URL is indexable and matches common search patterns.