Prostaglandin F Synthase (human, recombinant)

Prostaglandin F Synthase (human, recombinant)

CAT N°: 10007940
Price:

698.00 593.30

Human prostaglandin F synthase (PGFS) is a ~37 kDa monomeric protein with high sequence similarity to aldo-keto reductase family members.{8448} It exhibits two related primary activities, catalyzing the isomerization of PGH2 to PGF2? (PGH2 9,11-endoperoxide reductase activity), as well as the formation of 11?-PGF2? from PGD2 (PGD2 11-ketoreductase activity) in the presence of NADPH. The enzyme also exhibits reductase activities toward carbonyl compounds such at nitroacetophenone, nitrobenzaldehyde, and 9,10-phenanthrene quinine (PQ).{8022} Cayman’s human recombinant PGFS has been expressed and purified from an E.coli overexpression system. Enzyme activity was determined by monitoring the change in absorbance at 340 nm using PGD2 as the substrate and NADPH as the cofactor (PGD2 11-ketoreductase activity).

Territorial Availability: Available through Bertin Technologies only in France

  • Correlated keywords
    • 11.beta.-PGF2.alpha. 11b-PGF2alpha 9,11-endoperoxides 11-ketoreductases aldo-keto reductases human monomeric proteins catalyzing catalyzes isomerization PGH2 PGD2 NADPH nicotinamide adenine dinucleotide phosphates enzymes carbonyls nitroacetophenones nitrobenzaldehydes 9,10-phenanthrene quinine PQ E. coli gel electrophoresis commassie staining active
  • Product Overview:
    Human prostaglandin F synthase (PGFS) is a ~37 kDa monomeric protein with high sequence similarity to aldo-keto reductase family members.{8448} It exhibits two related primary activities, catalyzing the isomerization of PGH2 to PGF2? (PGH2 9,11-endoperoxide reductase activity), as well as the formation of 11?-PGF2? from PGD2 (PGD2 11-ketoreductase activity) in the presence of NADPH. The enzyme also exhibits reductase activities toward carbonyl compounds such at nitroacetophenone, nitrobenzaldehyde, and 9,10-phenanthrene quinine (PQ).{8022} Cayman’s human recombinant PGFS has been expressed and purified from an E.coli overexpression system. Enzyme activity was determined by monitoring the change in absorbance at 340 nm using PGD2 as the substrate and NADPH as the cofactor (PGD2 11-ketoreductase activity).

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