Phosphoglucomutase 1 Antikörper (AA 1-550)

Produktnummer ABIN7869465

Der Kaninchen Polyklonal anti-Phosphoglucomutase 1 Antikörper wird verwendet zum Nachweis von Phosphoglucomutase 1 in Proben von Human, Maus und Ratte. Er wurde validiert für WB und ELISA.

Kurzübersicht für Phosphoglucomutase 1 Antikörper (AA 1-550) (ABIN7869465)

Target: Phosphoglucomutase 1 (PGM1)

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Phosphoglucomutase 1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-Phosphoglucomutase 1 Antikörper

Bindungsspezifität: AA 1-550

Verwendungszweck: PGM1 Antibody / Phosphoglucomutase 1

Aufreinigung: Immunogen affinity purified

Immunogen: E.coli-derived human PGM1 recombinant protein (Position: M1-Q550) was used as the immunogen for the PGM1 antibody.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the PGM1 antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: After reconstitution, the PGM1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Details zu Phosphoglucomutase 1

Target: Phosphoglucomutase 1 (PGM1)

Andere Bezeichnung: PGM1

Hintergrund: PGM1 antibody recognizes phosphoglucomutase-1, a key enzyme in carbohydrate metabolism that catalyzes the reversible conversion of glucose-1-phosphate and glucose-6-phosphate. PGM1 functions at the crossroads of glycogen metabolism and glycolysis, influencing energy storage and utilization in multiple tissues including liver, muscle, and brain. The enzyme requires magnesium ions and a phosphoserine residue at its active site for catalytic activity. The PGM1 antibody is an essential reagent for biochemical and metabolic research, enabling analysis of energy metabolism, glycogen synthesis disorders, and enzymatic regulation across diverse physiological systems.

PGM1 is encoded by the PGM1 gene on human chromosome 1p31.3. It belongs to the phosphoglucomutase family, which includes several isoforms with distinct tissue distributions. The protein is composed of four structural domains forming a catalytic cleft that coordinates substrate binding and phosphoryl transfer. PGM1 deficiency is an inherited metabolic disorder characterized by impaired glycogen metabolism, hypoglycemia, and variable involvement of muscle and liver function. Mutations in the gene lead to partial or complete loss of enzyme activity, resulting in congenital disorder of glycosylation type It (PGM1-CDG).

The PGM1 antibody is commonly used in western blot and immunohistochemistry to detect the 61-63 kDa cytosolic protein. Expression studies demonstrate high levels in metabolically active tissues, including skeletal muscle, cardiac muscle, and hepatocytes. Immunofluorescence assays localize PGM1 primarily to the cytoplasm, consistent with its role in glucose metabolism. Functional studies have linked PGM1 activity to the regulation of glycogenolysis and the maintenance of glucose flux during fasting or exercise. Because of its importance in energy homeostasis, PGM1 serves as a biomarker for metabolic adaptation and carbohydrate-processing disorders.

PGM1 interacts with glycolytic enzymes and participates in metabolic channeling, facilitating efficient substrate transfer within enzymatic complexes. Recent work has shown that PGM1 expression may change in response to hypoxia, oxidative stress, and insulin signaling. NSJ Bioreagents provides a validated PGM1 antibody optimized for western blot, ELISA, and immunofluorescence applications. This reagent enables accurate quantification of enzyme levels in normal and disease models, supporting ongoing efforts to elucidate carbohydrate metabolism and its dysfunction in inherited and acquired disorders.

UniProt: P36871

Pathways: Cellular Glucan Metabolic Process