Render Target: STATIC
Render Timestamp: 2025-03-19T11:24:29.678Z
Commit: 779953b12a5930618aae6aca7c87fb286faeb1d7
XML generation date: 2025-03-07 13:19:50.101
Product last modified at: 2025-01-01T09:06:32.091Z
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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.

Spermine oxidase (F7Z4L) Rabbit mAb #35842

Filter:
  • WB

    Supporting Data

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

    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

    Spermine oxidase (F7Z4L) Rabbit mAb recognizes endogenous levels of total spermine oxidase protein.

    Species Reactivity:

    Mouse

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Pro276 of human spermine oxidase protein.

    Background

    Polyamines, including spermine, spermidine, and putrescine, are involved in many cellular processes, for example, cell proliferation, differentiation, apoptosis, the synthesis of proteins and nucleic acids, ion channel activity regulation, and the protection from oxidative injury (1). The cellular content of polyamines is tightly regulated; their biosynthesis is catalyzed by different enzymes including spermine synthase (SMS) and spermidine synthase (SRM), while the enzymes N1-acetylpolyamine oxidase (PAOX), spermidine/spermine N1-acetyltransferase 1 (SAT1) and spermine oxidase (SMOX) are involved in polyamine catabolism (1).

    SMOX is a flavoenzyme that catalyzes the oxidation of spermine to spermidine and is expressed in various tissues, mainly in brain and skeletal muscle (2,3). For several epithelial cancers, strong correlations have been established between chronic inflammation, cancer initiation and progression, and increased levels of SMOX, which lead to amplified H2O2 production, oxidative stress, and DNA damage (4). Mouse models with chronic overexpression of SMOX in cortical neurons show chronic astrocyte dysfunction, oxidative stress, and dysregulation of glutamatergic transmission, leading to epileptic seizures (3).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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