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PDPR anticorps (AA 155-655)

Cet anticorps Lapin Polyclonal détecte spécifiquement PDPR dans WB, ELISA et FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.
N° du produit ABIN7871012
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour PDPR anticorps (AA 155-655) (ABIN7871012)

Antigène

Voir toutes PDPR Anticorps
PDPR (Pyruvate Dehydrogenase Phosphatase Regulatory Subunit (PDPR))

Reactivité

Humain, Souris, Rat

Hôte

  • 12
Lapin

Clonalité

  • 12
Polyclonal

Conjugué

  • 7
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PDPR est non-conjugé

Application

  • 12
  • 8
  • 8
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Épitope

    • 8
    • 4
    • 2
    • 1
    AA 155-655

    Fonction

    PDPR Antibody / Pyruvate dehydrogenase phosphatase regulatory subunit

    Purification

    Immunogen affinity purified

    Immunogène

    E.coli-derived human PDPR recombinant protein (Position: E155-E655) was used as the immunogen for the PDPR antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the PDPR antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the PDPR antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    PDPR (Pyruvate Dehydrogenase Phosphatase Regulatory Subunit (PDPR))

    Autre désignation

    PDPR

    Sujet

    PDPR antibody detects Pyruvate dehydrogenase phosphatase regulatory subunit, a mitochondrial matrix protein encoded by the PDPR gene located on chromosome 16q22.1. PDPR acts as a regulatory subunit of the pyruvate dehydrogenase phosphatase (PDP) complex, which controls activity of the pyruvate dehydrogenase complex (PDC) - a critical enzyme in carbohydrate metabolism that links glycolysis to the tricarboxylic acid (TCA) cycle. PDPR is highly expressed in metabolically active tissues such as liver, heart, skeletal muscle, and kidney, where it modulates energy production and metabolic flexibility.

    PDPR functions by modulating the catalytic activity of PDP1 and PDP2 phosphatase subunits, facilitating dephosphorylation and reactivation of PDC. This regulation ensures efficient conversion of pyruvate to acetyl-CoA, thereby supporting ATP generation under nutrient-rich conditions. PDPR also influences glucose oxidation rates and metabolic adaptation during fasting, exercise, or insulin stimulation. Co-localization studies show PDPR associating with PDC and PDP1 in the mitochondrial matrix, maintaining dynamic control over carbohydrate flux.

    Structurally, PDPR contains an N-terminal domain involved in protein-protein interactions and a C-terminal alpha-helical region required for complex stability. It belongs to the pyruvate dehydrogenase regulatory protein family, which fine-tunes mitochondrial energy metabolism. The proteini 1/2s structural motifs enable binding with PDP catalytic subunits and coordination with mitochondrial targeting sequences for correct localization.

    Functionally, PDPR integrates metabolic and hormonal cues to maintain energy homeostasis. It plays a vital role in glucose utilization, mitochondrial respiration, and lipid oxidation balance. PDPR is regulated by insulin, glucagon, and nutrient availability, allowing cells to rapidly switch between carbohydrate and fatty acid metabolism. During embryonic development, PDPR supports energy demands of rapidly growing tissues, particularly cardiac and skeletal muscle. Pathway involvement includes the TCA cycle, oxidative phosphorylation, and insulin signaling pathways that coordinate energy metabolism.

    Dysregulation of PDPR activity is linked to metabolic diseases, including diabetes, obesity, and mitochondrial disorders. Reduced PDPR function leads to impaired PDC activation, resulting in accumulation of pyruvate and lactic acid, while overactivation can alter glucose oxidation balance. Genetic variants in PDPR have been associated with altered fasting glucose levels and insulin sensitivity. Because of its role in mitochondrial regulation, PDPR has also been studied in cancer metabolism, where metabolic reprogramming supports tumor cell proliferation.

    Immunohistochemical staining using PDPR antibody shows mitochondrial localization in liver, cardiac, and muscle cells. The PDPR antibody from NSJ Bioreagents is a valuable reagent for research on mitochondrial metabolism, energy regulation, and metabolic disease mechanisms.

    UniProt

    Q8NCN5
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