Conventional / global / constitutive KO
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Browse 1 Pfkm mouse model including knockout variants from ingenious targeting laboratory. Contact us for availability and fast turnaround.
Skeletal muscle glycolytic capacity rests on Pfkm, the mouse ortholog of human PFKM, which encodes the muscle subunit of phosphofructokinase 1 and dominates the tetramer in that tissue, where it catalyzes the committed, effectively irreversible ATP-dependent phosphorylation of fructose 6-phosphate and integrates AMP, ATP, citrate and fructose 2,6-bisphosphate signals into glycolytic rate. Recessive loss causes Tarui disease, glycogen storage disease type VII, in which exercise intolerance, cramps, myoglobinuria and compensated hemolysis follow from blocked muscle glycolysis, with the erythrocyte phenotype partial rather than complete because red cells contain M and L hybrid tetramers. Model design follows that tissue logic: a germline or muscle-restricted conditional null reproduces the metabolic myopathy, while patient-matched missense or splice knockins model residual activity and milder late-onset forms. Redundancy with Pfkl and Pfkp is real outside muscle. Choose the allele by endpoint, whether exercise challenge, glycogen accumulation, phosphorus magnetic resonance spectroscopy or hemolytic indices are the primary measures.
ingenious targeting laboratory offers 1 distinct Pfkm (PFKM) catalog mouse model, 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 |
|---|---|
| 1 Ready Catalog Line | 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 Pfkm (human PFKM). 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
1 Pfkm line with QC documentation and technical support.
Pfkm-KO
KnockoutKO/CKO mice, disease model mice
We have 1 Pfkm model available — including 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 Pfkm knockout mouse has the Pfkm gene permanently inactivated, enabling loss of function studies.
Jump to catalog backed pages for Pfkm organized by modification type. Each URL is indexable and matches common search patterns.