Conventional / global / constitutive KO
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Browse 4 Pdgfra mouse models including conditional knockout, knockin variants — in stock and ready to ship from ingenious targeting laboratory. Available as Pdgfra conditional knockout mouse, Pdgfra knockin mouse. Request a quote within 24 hours.
Pdgfra encodes the mouse ortholog of human PDGFRA, a class III receptor tyrosine kinase that binds PDGF-A, PDGF-C, and PDGF-B as homodimers or as heterodimers with PDGFRB, then autophosphorylates to engage PI3K, phospholipase C gamma, SHP2, and RAS-ERK, directing cranial and cardiac neural crest, oligodendrocyte precursor, and gastrointestinal mesenchymal development. Oncogenic activation takes several distinct forms: activation loop D842V and juxtamembrane mutations in KIT wild-type gastrointestinal stromal tumor, which resist imatinib but respond to avapritinib, FIP1L1-PDGFRA fusions in hypereosinophilic myeloid neoplasms, and amplification in diffuse midline glioma. Germline nulls die in midgestation with craniofacial and cardiac defects, exactly as in the classic Patch deletion, so hotspot knockins should be conditional or inducible, and conditional nulls serve adult mesenchymal and oligodendrocyte questions. The paralog Pdgfrb heterodimerizes and shares ligands, so single-locus deletion can be buffered in perivascular compartments; choose Cre drivers by lineage and read out tumor latency or inhibitor response.
ingenious targeting laboratory offers 4 distinct Pdgfra (PDGFRA) catalog mouse models, featuring conditional 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 |
|---|---|
| 4 Ready Catalog Lines | Conditional Knockout (cKO) |
| Custom Model Generation | Constitutive Knockout (KO) on request |
| 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 Pdgfra (human PDGFRA). 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
4 Pdgfra lines with QC documentation and technical support. Pdgfra floxed mice use loxP flanked alleles for Cre dependent tissue specific knockout.
Pdgfra-Flox
Conditional KnockoutKO/CKO mice, disease model mice
Pdgfra-CreERT2
KnockinCre/Dre Toolbox of Mice
Pdgfra-Dre
KnockinCre/Dre Toolbox of Mice
Pdgfra-EGFP-CreERT2
KnockinCre/Dre Toolbox of Mice, fluorescent mouse
We have 4 Pdgfra models in stock — including Conditional Knockout, Knockin 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 Pdgfra conditional knockout (floxed) mouse carries loxP sites flanking a critical exon of Pdgfra, allowing Cre recombinase dependent deletion in specific tissues or at specific timepoints. Pdgfra knockin models carry a precisely inserted sequence at the Pdgfra locus, useful for reporter, tag, or humanization studies.
Jump to catalog backed pages for Pdgfra organized by modification type. Each URL is indexable and matches common search patterns.