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Product Name
PGAM2 antibody
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Description
PGAM2 Rabbit Polyclonal antibody. Positive WB detected in mouse skeletal muscle tissue. Positive IHC detected in human skin tissue, human brain tissue, human heart tissue, human kidney tissue, human liver tissue, human lung tissue, human ovary tissue, human spleen tissue, human testis tissue. Observed molecular weight by Western-blot: 28-29kd
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Tested applications
ELISA, WB, IHC
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Species reactivity
Human, Mouse; other species not tested.
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Alternative names
BPG dependent PGAM 2 antibody; PGAM M antibody; PGAM2 antibody; PGAMM antibody; Phosphoglycerate mutase 2 antibody
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Isotype
Rabbit IgG
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Preparation
This antibody was obtained by immunization of PGAM2 recombinant protein (Accession Number: NM_000290). Purification method: Antigen affinity purified.
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Clonality
Polyclonal
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Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
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Storage instructions
Store at -20℃. DO NOT ALIQUOT
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Applications
Recommended Dilution:
WB: 1:500-1:5000
IHC: 1:20-1:200
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Validations
mouse skeletal muscle tissue were subjected to SDS PAGE followed by western blot with Catalog No:113777(PGAM2 antibody) at dilution of 1:1500
Immunohistochemical of paraffin-embedded human skin using Catalog No:113777(PGAM2 antibody) at dilution of 1:100 (under 10x lens)
Immunohistochemical of paraffin-embedded human skin using Catalog No:113777(PGAM2 antibody) at dilution of 1:100 (under 40x lens)
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Background
Phosphoglycerate mutase (PGAM), an important enzyme in the glycolytic pathway, catalyzes the transfer of a phosphate group between the 2 and the 3 positions of glyceric acid. The muscle-specific isoform (type M, PGAM2) of phosphoglycerate mutase (PGAM) is a housekeeping enzyme and it catalyzes the conversion of 3-phosphoglycerate into 2-phosphoglycerate in the glycolysis process to release energy. It is encoded by the Pgam2 gene. In addition, it is demonstrated that PGAM2 locates both in cytoplasm and nuclei, and takes part in the glycometabolism process of cytoplasm and nuclei(PMID: 18499067). Defects in PGAM2 are the cause of glycogen storage disease type 10 (GSD10).
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