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Human PFK1 / PFKM Protein (His & GST Tag)

ATP-PFK,GSD7,PFK-1,PFK1,PFKA,PFKX,PPP1R122

Catalog Number P14133-H20B
Organism Species Human
Host Baculovirus-Insect Cells
Synonyms ATP-PFK,GSD7,PFK-1,PFK1,PFKA,PFKX,PPP1R122
Molecular Weight The recombinant human PFKM /GST chimera consists of 1016 amino acids and has a calculated molecular mass of 112.9 kDa. The recombinant protein migrates as an approximately 113 kDa band in SDS-PAGE under reducing conditions.
predicted N Met
SDS-PAGE
Purity > 90 % as determined by SDS-PAGE
Protein Construction A DNA sequence encoding the human PFKM (P08237-1) (Thr2-Val780) was fused with the N-terminal polyhistidine-tagged GST tag at the N-terminus.
Bio-activity Kinase activity untested
Research Area Cancer |Signal transduction |Metabolism |Pathways and Processes |Metabolic signaling pathways |Carbohydrate metabolism |
Formulation Supplied as sterile 20mM Tris, 500mM NaCl, pH 8.5, 10% glycerol
1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.
Background PFK1, also known as PFKM, is a regulatory glycolytic enzyme. PFK1 converts fructose 6-phosphate and ATP into fructose 1,6-bisphosphate (through PFK-1), fructose 2,6-bisphosphate (through PFK-2) and ADP. It is a muscle-type isozyme. There are three phosphofructokinase isozymes 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. Mutations in PFK1 gene have been related with glycogen storage disease type VII, also identified as Tarui disease.
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