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Anti-DMPO Nitrone Adduct Antibody

Mouse Monoclonal Antibody specific to DMPO Nitrone Adduct

Product Specifications

CAS Number

9007-83-4

Product Name Alternative

Anti-DMPO Nitrone Adduct Mouse Monoclonal Antibody

Host

Mouse

Reactivity

All

Immunogen

5,5-dimethyl-2-(8-octanoic acid)-1-pyrrolone-N-oxide conjugated to ovalbumin.

Target

DMPO Nitrone Adduct

Clonality

Monoclonal

Isotype

IgG1

Type

Antibody

Applications

WB, IHC, ICC/IF, IP, ELISA, AM

Field of Research

DNA

Purification Method

Purified by Protein G affinity chromatography

Concentration

Lot Specific

Dilution

Dilute in PBS or medium that is identical to that used in the assay system.

Format

Purified

Form

Liquid

Buffer

Phosphate Buffered Saline

Additionnal Information

Immunoblotting: use at 1-10ug/mL. <br><br>Immunofluorescence: use at10ug/mL. <br><br>These are recommended concentrations; <br><br>Enduser should determine optimal concentrations for their applications <br><br>ELISA: use at 1-10ug/mL <br><br>Positive control: DMPO nitrone adducts of metmyoglobin.

Storage Conditions

This antibody is stable for at least one (1) year at -20°C. Avoid multiple freeze-thaw cycles.

Specificity

This antibody recognizes DMPO, DMPO-octanoic acid, DMPO-protein adducts, and DMPO-DNA adducts. It does not cross-react with non-adducted proteins or DNA. Species independent.

Formulation

PBS, pH 7.4, 50% glycerol, 0.09% sodium azide.

Buffer pH

pH 7.4

Target Background

Free radicals are highly reactive and generally short-lived species. Hence, most studies of free radicals have been restricted to analysis of end products formed following their interaction with cellular biomolecules. One technology that has permitted direct study of free radicals is electron spin resonance (ESR). For very short lived radicals, spin traps have been employed to generate longer lived radicals that are more amenable to ESR analysis. The most widely used of these spin traps is 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). The reaction of DMPO with a protein radical gives rise to a nitroxide radical which can be disproportionate to hydrozylamine and nitrone adducts. Of these species, only the nitrone adduct can be considered stable.

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