Full Product Name
PGAM2 Rabbit Polyclonal
Product Gene Name
anti-PGAM2 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Species Reactivity
Human, Mouse
Purity/Purification
>=95% as determined by SDS-PAGE
Immunogen Affinity Purified
Immunogen
Phosphoglycerate mutase 2 (muscle)
Preparation and Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20 degree C for 24 months (Avoid repeated freeze / thaw cycles.)
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of anti-PGAM2 antibody 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.
Applications Tested/Suitable for anti-PGAM2 antibody
ELISA (EIA), Western Blot (WB)
NCBI/Uniprot data below describe general gene information for PGAM2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_000281.2
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NCBI GenBank Nucleotide #
NM_000290.3
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UniProt Related Accession #
P15259[Other Products]
Molecular Weight
28,766 Da
NCBI Official Full Name
phosphoglycerate mutase 2
NCBI Official Synonym Full Names
phosphoglycerate mutase 2
NCBI Official Symbol
PGAM2 [Similar Products]
NCBI Official Synonym Symbols
GSD10; PGAMM; PGAM-M
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NCBI Protein Information
phosphoglycerate mutase 2
UniProt Protein Name
Phosphoglycerate mutase 2
UniProt Synonym Protein Names
BPG-dependent PGAM 2; Muscle-specific phosphoglycerate mutase; Phosphoglycerate mutase isozyme M; PGAM-M
Protein Family
Phosphoglycerate mutase
UniProt Gene Name
PGAM2 [Similar Products]
UniProt Synonym Gene Names
PGAMM; PGAM-M [Similar Products]
UniProt Entry Name
PGAM2_HUMAN
NCBI Summary for PGAM2
Phosphoglycerate mutase (PGAM) catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). This gene encodes muscle-specific PGAM subunit. Mutations in this gene cause muscle phosphoglycerate mutase eficiency, also known as glycogen storage disease X. [provided by RefSeq, Sep 2009]
UniProt Comments for PGAM2
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; Isomerase; EC 5.4.2.11; EC 5.4.2.4; Phosphatase (non-protein); EC 3.1.3.13
Chromosomal Location of Human Ortholog: 7p13-p12
Cellular Component: cytosol; nucleus
Molecular Function: 2,3-bisphosphoglycerate-dependent phosphoglycerate mutase activity; bisphosphoglycerate mutase activity; bisphosphoglycerate phosphatase activity; cofactor binding; phosphoglycerate mutase activity
Biological Process: dephosphorylation; gluconeogenesis; glycolysis; Notch signaling pathway; regulation of pentose-phosphate shunt; response to mercury ion; spermatogenesis; striated muscle contraction
Disease: Glycogen Storage Disease X
Research Articles on PGAM2
1. These results reveal a mechanism of PGAM2 regulation and NADPH homeostasis in response to oxidative stress that impacts cell proliferation and tumor growth.
Precautions
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