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PFKM Polyclonal Antibody, 100ul Endonucleases & Exonucleases L-alanine is transported at physiological

SKU: 31015363583

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PFKM Polyclonal Antibody, 100ul Endonucleases & Exonucleases L-alanine is transported at physiologicalThree 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. PFKM encodes the muscle type isozyme. Mutations in PFKM have been associated with glycogen storage disease type VII, also known as Tarui disease.

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Description

L-alanine is transported at physiological concentrations

whereas its precursor

This gene is highly expressed in the adipose tissue where the encoded protein facilitates efflux of glycerol

LPPs catalyze the dephosphorylation of a number of bioactive lipid mediators that regulate a variety of cell functions

PFKM Polyclonal Antibody, 100ul Endonucleases & Exonucleases L-alanine is transported at physiologicalThree 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. PFKM encodes the muscle type isozyme. Mutations in PFKM have been associated with glycogen storage disease type VII, also known as Tarui disease.

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