Conventional / global / constitutive KO
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Browse 1 Ubqln2 mouse model including knockout variants from ingenious targeting laboratory. Contact us for availability and fast turnaround.
Ubiquilin-2, encoded by X-linked mouse Ubqln2 and orthologous to human UBQLN2, is a proteasome shuttle factor with an N-terminal ubiquitin-like domain that docks the 26S proteasome, central STI1-like chaperone regions that bind hydrophobic and transmembrane segments, a primate-specific PXX repeat region, and a C-terminal UBA domain that captures polyubiquitinated substrates. It thereby delivers misfolded and ribosome-quality-control substrates for degradation, participates in autophagosome maturation, and undergoes phase separation into stress granules. Dominant mutations concentrated in the PXX repeat, including P497H, P506T, and P525S, cause X-linked ALS and frontotemporal dementia with ubiquilin-2-positive inclusions. Because that repeat region is absent in rodents, humanized knockin alleles are essentially required for faithful variant modeling rather than murine point mutations. Conditional or constitutive nulls remain useful for proteostasis flux questions, and functional overlap with Ubqln1 and Ubqln4 means compound alleles may be needed when total shuttle capacity is the endpoint.
ingenious targeting laboratory offers 1 distinct Ubqln2 (UBQLN2) catalog mouse model, 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 |
|---|---|
| 1 Ready Catalog Line | 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 Ubqln2 (human UBQLN2). 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
1 Ubqln2 line with QC documentation and technical support.
Ubqln2-KO
KOKO
The exon1 of Ubqln2 gene was deleted to generate Ubqln2 knockout mouse.
We have 1 Ubqln2 model 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 Ubqln2 knockout mouse has the Ubqln2 gene permanently inactivated, enabling loss of function studies.
Jump to catalog backed pages for Ubqln2 organized by modification type. Each URL is indexable and matches common search patterns.
Send the Ubqln2 line to a U.S. barrier facility for colony maintenance, cohort production, and complex breeding schemes through mouse breeding services.