|Other Names||Phosphoglycerate mutase 2, BPG-dependent PGAM 2, Muscle-specific phosphoglycerate mutase, Phosphoglycerate mutase isozyme M, PGAM-M, PGAM2, PGAMM|
|Format||Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.|
|Storage||Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.|
|Precautions||This product is for research use only. Not for use in diagnostic or therapeutic procedures.|
|Function||Interconversion of 3- and 2-phosphoglycerate with 2,3- bisphosphoglycerate as the primer of the reaction. Can also catalyze the reaction of EC 220.127.116.11 (synthase) and EC 18.104.22.168 (phosphatase), but with a reduced activity.|
|Tissue Location||In mammalian tissues there are two types of phosphoglycerate mutase isozymes: type-M in muscles and type-B in other tissues|
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Provided below are standard protocols that you may find useful for product applications.
Phosphoglycerate mutase (PGAM) catalyzes the reversiblereaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate(2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzymecontaining, in different tissues, different proportions of aslow-migrating muscle (MM) isozyme, a fast-migrating brain (BB)isozyme, and a hybrid form (MB). PGAM2 encodes muscle-specificPGAM subunit. Mutations in this gene cause muscle phosphoglyceratemutase eficiency, also known as glycogen storage disease X.
Hadjigeorgiou, G.M., et al. Neuromuscul. Disord. 9 (6-7), 399-402 (1999) :Tsujino, S., et al. Am. J. Hum. Genet. 52(3):472-477(1993)Castella-Escola, J., et al. Gene 91(2):225-232(1990)Castella-Escola, J., et al. Hum. Genet. 84(2):210-212(1990)Tsujino, S., et al. J. Biol. Chem. 264(26):15334-15337(1989)
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