![WB analysis of HepG2 lysate (30ug) using PFKM antibody [AT2F11] at the indicated dilutions. WB analysis of HepG2 lysate (30ug) using PFKM antibody [AT2F11] at the indicated dilutions.](https://www.genetex.com/upload/website/prouct_img/normal/GTX53761/GTX53761_WB_w_23060900_814.webp)
WB analysis of HepG2 lysate (30ug) using PFKM antibody [AT2F11] at the indicated dilutions.
PFKM antibody [AT2F11]
GTX53761
Overview
- SupplierGeneTex
- Product NameFructose 6 Phosphate Kinase antibody [AT2F11]
- Delivery Days Customer9
- Application Supplier NoteThe antibody has been tested by ELISA, Western blot analysis to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results. Recommended dilution range for Western blot analysis is 1:500 ~ 1:2000. Recommended starting dilution is 1:2000.
- ApplicationsWestern Blot, ELISA
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDAT2F11
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID5213
- Target namePFKM
- Target descriptionphosphofructokinase, muscle
- Target synonyms6-phosphofructo-1-kinase; 6-phosphofructokinase type A; 6-phosphofructokinase, muscle type; ATP-dependent 6-phosphofructokinase, muscle type; ATP-PFK; GSD7; PFK1; PFK-1; PFKA; PFK-A; PFKX; phosphofructo-1-kinase isozyme A; phosphofructokinase 1; phosphofructokinase, polypeptide X; phosphofructokinase-M; phosphohexokinase; PPP1R122; protein phosphatase 1, regulatory subunit 122
- HostMouse
- IsotypeIgG2a
- Protein IDP08237
- Protein NameATP-dependent 6-phosphofructokinase, muscle type
- Scientific DescriptionThree phosphofructokinase isozymes exist in humans: muscle, liver and platelet. These isozymes function as subunits of the mammalian tetramer phosphofructokinase, which catalyzes the phosphorylation of fructose-6-phosphate to fructose-1,6-bisphosphate. Tetramer composition varies depending on tissue type. This gene encodes the muscle-type isozyme. Mutations in this gene have been associated with glycogen storage disease type VII, also known as Tarui disease. Alternatively spliced transcript variants have been described.[provided by RefSeq, Nov 2009]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203