Conventional / global / constitutive KO
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Browse 3 Met mouse models including conditional knockout, knockin, knockout variants — in stock and ready to ship from ingenious targeting laboratory. Available as Met conditional knockout mouse, Met knockin mouse, Met knockout mouse. Request a quote within 24 hours.
Receptor tyrosine kinase MET, encoded in mouse by Met, is the single-pass receptor for hepatocyte growth factor, comprising a SEMA domain, PSI and IPT repeats, and a cytoplasmic kinase domain whose phosphorylated Y1349 and Y1356 residues recruit GAB1 and GRB2 to activate RAS-ERK, PI3K-AKT, and STAT3, driving epithelial morphogenesis, hepatocyte survival, and myoblast migration. Oncogenic activation occurs through amplification, exon 14 skipping that removes the CBL-binding juxtamembrane degron and stabilizes the receptor, kinase domain germline mutations such as M1250T in hereditary papillary renal carcinoma, and TPR-MET rearrangement. Germline nulls die near midgestation from placental and hepatic failure, so conditional deletion is required for regeneration and tumor dependency studies, while exon 14 skipping or kinase domain knockins model ligand-independent signaling and inhibitor response. Since HGF binding is species selective, humanized MET or ligand-humanized alleles are essential for antibody and antibody-drug conjugate testing; pair these with epithelial Cre lines matched to the intended tumor lineage.
ingenious targeting laboratory offers 3 distinct Met (MET) 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 |
|---|---|
| 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
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Knockout, conditional, knockin, humanized, and related paths for Met (human MET). 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 Met lines with QC documentation and technical support. Met floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
Peer reviewed work involving Met (MET) from ITL supported projects.
We have 3 Met 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 Met knockout mouse has the Met gene permanently inactivated, enabling loss of function studies. A Met conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Met, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints. Met knockin models carry a precisely inserted sequence at the Met locus, useful for reporter, tag, or humanization studies.
Jump to catalog backed pages for Met organized by modification type. Each URL is indexable and matches common search patterns.