Conventional / global / constitutive KO
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Browse 2 U2af1 mouse models including conditional knockout, knockout variants from ingenious targeting laboratory. Available as U2af1 conditional knockout mouse, U2af1 knockout mouse. Contact us for availability and fast turnaround.
Recognition of the 3 prime splice site depends on U2af1, the mouse ortholog of human U2AF1, the small subunit of the U2 auxiliary factor heterodimer, which uses two CCCH zinc fingers to contact the invariant AG dinucleotide and flanking nucleotides while its U2AF homology motif binds U2AF2 and licenses U2 snRNP loading at the branch point. Myeloid disease mutations are heterozygous and mutually exclusive with SF3B1 and SRSF2 lesions, with S34F and S34Y altering preference at the position three nucleotides upstream of the AG and Q157P or Q157R altering the position immediately downstream, producing distinct cassette exon and intron retention programs rather than global splicing failure; identical substitutions recur in lung adenocarcinoma. Because complete loss is not tolerated, the correct design is a conditional or doxycycline-inducible heterozygous hotspot knockin at the endogenous locus, induced with Mx1-cre or Vav1-cre to capture dysplastic hematopoiesis. Match allele to endpoint, whether isoform mapping, competitive repopulation, or spliceosome modulator sensitivity.
ingenious targeting laboratory offers 2 distinct U2af1 (U2AF1) 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 U2af1 (human U2AF1). 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 U2af1 lines with QC documentation and technical support. U2af1 floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
Peer reviewed work involving U2af1 (U2AF1) from ITL supported projects.
We have 2 U2af1 models available — including Conditional Knockout, 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 U2af1 knockout mouse has the U2af1 gene permanently inactivated, enabling loss of function studies. A U2af1 conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of U2af1, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints.
Jump to catalog backed pages for U2af1 organized by modification type. Each URL is indexable and matches common search patterns.