Conventional / global / constitutive KO
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Browse 2 Atp13a2 mouse models including knockout variants from ingenious targeting laboratory. Contact us for availability and fast turnaround.
Atp13a2, ortholog of human ATP13A2 (PARK9), encodes a P5B-type transport ATPase resident in late endosomes and lysosomes that exports polyamines, principally spermine, from the lumen to the cytosol using an N-terminal lipid-binding domain that recognizes phosphatidic acid and phosphoinositides for membrane targeting. Recessive truncating and misfolding alleles cause Kufor-Rakeb juvenile parkinsonism and neuronal ceroid lipofuscinosis, with loss of function producing lysosomal alkalinization, impaired cathepsin maturation, spermine-driven lysosomal rupture, and secondary accumulation of α-synuclein and lipofuscin. Conditional nulls crossed to Dat-Cre or Slc6a3-Cre isolate dopaminergic cell-autonomous degeneration, whereas a patient missense knockin distinguishes catalytic failure from ER retention and degradation of misfolded protein, and humanization supports chaperone or antisense screening against the human coding sequence. The paralogs Atp13a3, Atp13a4 and Atp13a5 transport overlapping polyamine substrates in other compartments, so quantify them before interpreting a mild null; age animals well past twelve months for lipofuscin and gliosis endpoints.
ingenious targeting laboratory offers 2 distinct Atp13a2 (ATP13A2) 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 Atp13a2 (human ATP13A2). 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
Specify rat on quote
Specify rabbit on quote
Background substrain on quote
Background strain on quote
We have 2 Atp13a2 models available — including 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 Atp13a2 knockout mouse has the Atp13a2 gene permanently inactivated, enabling loss of function studies.
Jump to catalog backed pages for Atp13a2 organized by modification type. Each URL is indexable and matches common search patterns.