Phosphoglycerate mutase 2; BPG-dependent PGAM 2; Muscle-specific phosphoglycerate mutase; Phosphoglycerate mutase isozyme M; PGAM-M; Pgam2; 3.1.3.13

For Research Use Only. Not for use in diagnostic procedures.

Store at 4 degree C

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Small volumes of Pgam2 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS9427667 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Phosphoglycerate mutase 2 (Pgam2) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing Pgam2. The ELISA analytical biochemical technique of the MBS9427667 kit is based on Pgam2 antibody-Pgam2 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect Pgam2 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, Pgam2. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).

28,755 Da

phosphoglycerate mutase 2

phosphoglycerate mutase 2

Phosphoglycerate mutase 2

PGAM-M??[Similar Products]

catalyzes the interconversion of 2-phospho-D-glycerate and 3-phospho-D-glycerate [RGD, Feb 2006]

PGAM2: Interconversion of 3- and 2-phosphoglycerate with 2,3- bisphosphoglycerate as the primer of the reaction. Can also catalyze the reaction of EC 5.4.2.4 (synthase) and EC 3.1.3.13 (phosphatase), but with a reduced activity. Defects in PGAM2 are the cause of glycogen storage disease type 10 (GSD10). A metabolic disorder characterized by myoglobinuria, increased serum creatine kinase levels, decreased phosphoglycerate mutase activity, myalgia, muscle pain, muscle cramps and excercise intolerance. Belongs to the phosphoglycerate mutase family. BPG- dependent PGAM subfamily.

Protein type: Carbohydrate Metabolism - glycolysis and gluconeogenesis; EC 3.1.3.13; EC 5.4.2.11; EC 5.4.2.4; Isomerase; Phosphatase (non-protein)

Chromosomal Location of Human Ortholog: 14q21

Cellular Component: cytosol; nucleus

Molecular Function: 2,3-bisphosphoglycerate-dependent phosphoglycerate mutase activity; cofactor binding; phosphoglycerate mutase activity

Biological Process: gluconeogenesis; glycolysis; Notch signaling pathway; regulation of pentose-phosphate shunt; response to inorganic substance; response to mercury ion; spermatogenesis; striated muscle contraction

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