PGAM1 Antikörper (AA 1-254)

Produktnummer ABIN5542084

Dieses Anti-PGAM1-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von PGAM1 in WB, ICC, IF, FACS und EIA. Geeignet für Human.

Kurzübersicht für PGAM1 Antikörper (AA 1-254) (ABIN5542084)

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

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser PGAM1 Antikörper ist unkonjugiert

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

Klon: AT1G4

Produktdetails anti-PGAM1 Antikörper

Bindungsspezifität: AA 1-254

Aufreinigung: Protein-A affinity chromatography

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

Isotyp: IgG2a

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Haltbarkeit: 12 months

Details zu PGAM1

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

Andere Bezeichnung: pgam1

Hintergrund: 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