Render Target: SSR
Render Timestamp: 2024-12-19T21:29:54.844Z
Commit: f2d32940205a64f990b886d724ccee2c9935daff
XML generation date: 2024-09-30 01:59:09.879
Product last modified at: 2024-11-14T17:45:07.618Z
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PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

PGM1 (E2I5G) Rabbit mAb #68036

Filter:
  • WB

    Supporting Data

    REACTIVITY H M R
    SENSITIVITY Endogenous
    MW (kDa) 62
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    Species Cross-Reactivity Key:
    • H-Human 
    • M-Mouse 
    • R-Rat 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000

    Storage

    Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

    Protocol

    Specificity / Sensitivity

    PGM1 (E2I5G) Rabbit mAb recognizes endogenous levels of total PGM1 protein. This antibody does not cross-react with PGM2 protein.

    Species Reactivity:

    Human, Mouse, Rat

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Gly279 of human PGM1 protein.

    Background

    Phosphoglucomutase-1 (PGM1) catalyzes the interconversion of glucose 1-phosphate (G-1-P) and glucose 6-phosphate (G-6-P) in the breakdown and synthesis of glycogen. PGM1 expression is downregulated in hepatocellular carcinoma (HCC), suppressing the glycogen synthesis pathway and increasing glucose entry into glycolysis to support cancer proliferation (1). Studies show that TGF-β1 released by ovarian cancer cells induces p38 MAPK signaling in neighboring cancer-associated fibroblasts (CAFs), releasing cytokines and chemokines from CAFs. These cytokines and chemokines promote glycogen mobilization in ovarian cancer cells, stimulating cancer cell proliferation, invasion, and metastasis. Phosphorylation of Tyr353 on PGM1 is essential for its enzymatic activity and glycogen mobilization induced by CAFs (2).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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