PGAM1 anticorps (AA 1-254)

N° du produit ABIN5542084

Cet anticorps anti-PGAM1 est un anticorps Souris Monoclonal détectant PGAM1 dans WB, ICC, IF, FACS et EIA. Adapté pour Humain.

Aperçu rapide pour PGAM1 anticorps (AA 1-254) (ABIN5542084)

Antigène: PGAM1 (phosphoglycerate Mutase 1 (Brain) (PGAM1))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp PGAM1 est non-conjugé

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF), Flow Cytometry (FACS), Enzyme Immunoassay (EIA)

Clone: AT1G4

Détail du produit anti-PGAM1 anticorps

Épitope: AA 1-254

Purification: Protein-A affinity chromatography

Immunogène: Recombinant human PGAM1 (1-254aa) purified from E. coli.

Isotype: IgG2a

Information d'application

Indications d'application: The antibody has been tested by ELISA, Western blot analysis, ICC/IF and Flow cytometry to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid. In Phosphate-Buffered Saline ( pH 7.4) with 0.02 % Sodium Azide, 10 % Glycerol.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. Shelf life: one year from despatch.

Date de péremption: 12 months

Détails sur PGAM1

Antigène: PGAM1 (phosphoglycerate Mutase 1 (Brain) (PGAM1))

Autre désignation: pgam1

Sujet: PGAM1 belongs to the phosphoglycerate mutase family. This protein is important components of glucose and 2,3-BPGA (2,3-bisphosphoglycerate) metabolism and 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). Mutations in this protein cause muscle phosphoglycerate mutase eficiency, also known as glycogen storage disease X.

UniProt: P18669

Pathways: Regulation of Carbohydrate Metabolic Process