Conventional / global / constitutive KO
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Browse 3 Sqstm1 mouse models including conditional knockout, knockout variants — in stock and ready to ship from ingenious targeting laboratory. Available as Sqstm1 conditional knockout mouse, Sqstm1 knockout mouse. Request a quote within 24 hours.
p62, the product of mouse Sqstm1 and ortholog of human SQSTM1, is a multidomain signaling adaptor and selective autophagy receptor built from an N-terminal PB1 domain that self-oligomerizes and binds NBR1 and atypical PKCs, a ZZ zinc finger, a TRAF6 binding region, an LC3-interacting region, a KEAP1-interacting region, and a C-terminal UBA domain that captures ubiquitinated cargo. By bridging polyubiquitinated substrates to LC3 on the phagophore, p62 drives aggrephagy and mitophagy, while sequestering KEAP1 to activate NRF2 antioxidant transcription and scaffolding NF-kappaB signaling. SQSTM1 mutations, mostly clustered in the UBA domain, cause Paget disease of bone, ALS with frontotemporal dementia, and distal myopathy. Constitutive knockout mice are viable but develop mature-onset obesity, insulin resistance, and age-dependent neurodegeneration, so metabolic confounds argue for conditional deletion with neuronal or microglial Cre drivers, while UBA or LIR point knockins cleanly separate cargo binding from NRF2 and NF-kappaB functions.
ingenious targeting laboratory offers 3 distinct Sqstm1 (SQSTM1) 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 |
|---|---|
| 3 Ready Catalog Lines | Conditional Knockout (cKO) |
| Custom Model Generation | Constitutive Knockout (KO) |
| Advanced Modifications | Humanized, Knockin, Transgenic |
Knockout
Conditional knockout
Knockin
Humanized
Transgenic / overexpression
Prefer the order form? Order. Need an allele that is not listed? Request a quote.
Knockout, conditional, knockin, humanized, and related paths for Sqstm1 (human SQSTM1). 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
3 Sqstm1 lines with QC documentation and technical support. Sqstm1 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
We have 3 Sqstm1 models in stock — including Conditional Knockout, 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 Sqstm1 knockout mouse has the Sqstm1 gene permanently inactivated, enabling loss of function studies. A Sqstm1 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Sqstm1, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Sqstm1 organized by modification type. Each URL is indexable and matches common search patterns.