Conventional / global / constitutive KO
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Browse 2 Notch2 mouse models including conditional knockout, knockout variants — in stock and ready to ship from ingenious targeting laboratory. Available as Notch2 conditional knockout mouse, Notch2 knockout mouse. Request a quote within 24 hours.
Ligand-dependent proteolysis governs Notch2, the mouse ortholog of human NOTCH2, which encodes a receptor with the same modular architecture as Notch1, using EGF repeats for Dll and Jag engagement, a negative regulatory region stabilized by S1 furin processing, sequential Adam10 and gamma-secretase cleavage, and an intracellular domain that partners with Rbpj and Maml before PEST-directed degradation. Its human genetics run in both directions: haploinsufficiency and hypomorphic alleles cause Alagille syndrome with bile duct paucity, whereas PEST-truncating mutations that stabilize the intracellular domain cause Hajdu-Cheney syndrome with acro-osteolysis, and NOTCH2 lesions recur in marginal zone lymphoma. Homozygous nulls die in mid-gestation, while the hypomorphic allele survives with cardiac, renal, and hepatic defects, so conditional deletion is the standard route for biliary, splenic, and skeletal studies. A PEST truncation knockin models gain-of-function bone disease, and receptor-specific humanization supports paralog-selective antibodies. Notch1 overlaps in liver and B cell compartments, making Notch1 and Notch2 compound alleles necessary for full penetrance.
ingenious targeting laboratory offers 2 distinct Notch2 (NOTCH2) 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 Notch2 (human NOTCH2). 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
2 Notch2 lines with QC documentation and technical support. Notch2 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
Peer reviewed work involving Notch2 (NOTCH2) from ITL supported projects.
We have 2 Notch2 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 Notch2 knockout mouse has the Notch2 gene permanently inactivated, enabling loss of function studies. A Notch2 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Notch2, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for Notch2 organized by modification type. Each URL is indexable and matches common search patterns.