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8-OHdG (DNA/RNA Damage) Antibody

Art. -Nr.: HY-P81140
COA User Guide for Antibodies Technical Support

8-OHdG (DNA/RNA Damage) Antibody is a Rabbit-derived and non-conjugated IgG polyclonal antibody, targeting to 8-OHdG (DNA/RNA Damage).

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Top Publications Citing Use of Products

    8-OHdG (DNA/RNA Damage) Antibody purchased from MCE. Usage Cited in: Engineering. 2025 Oct 31.

    8-OHdG(1;300) immunofluorescence staining in the temporal cortical region of mouse brain tissue.

    8-OHdG (DNA/RNA Damage) Antibody purchased from MCE. Usage Cited in: ACS Appl Mater Interfaces. 2025 Oct 1;17(39):54484-54495.  [Abstract]

    Representative immunofluorescence images of mouse lung tissue sections stained for the oxidative stress marker 8-OHdG.

    8-OHdG (DNA/RNA Damage) Antibody purchased from MCE. Usage Cited in: Basic Res Cardiol. 2025 Sep 16.  [Abstract]

    8-hydroxy-2'-deoxyguanosine (8-OHdG) immunofluorescence with MFI in mouse 3-hit hearts;

    8-OHdG (DNA/RNA Damage) Antibody purchased from MCE. Usage Cited in: J Ethnopharmacol. 2025 Dec 30:360:121126.  [Abstract]

    Representative immunohistochemical staining of 8-OHdG in mouse liver tissues.

    8-OHdG (DNA/RNA Damage) Antibody purchased from MCE. Usage Cited in: Mol Oncol. 2025 Jul 13.  [Abstract]

    Representative images (left) and quantification (right) of 8-oxo-dG–positive nuclei (green) in MDA-MB231 cells after 24 h of the indicated treatments. Nuclei were counterstained with DAPI (blue). Quantification represents the percentage of 8-oxo-dG–positive cells, with a minimum of 200 nuclei counted per independent experiment.
    • WB: Western Blot;
    • IHC-P: Immunohistochemistry-Paraffin;
    • IHC-F: Immunohistochemistry-Frozen;
    • ICC/IF: Immunocytochemistry/Immunofluorescence;
    • IF-Tissue: Immunofluorescence-Tissue;
    • mIHC: Multiplex Immunohistochemical;
    • IP: Immunoprecipitation;
    • ChIP: Chromatin Immunoprecipitation;
    • FC: Flow Cytometry;
    • ELISA: Enzyme Linked Immunosorbent Assay
    • Product Detail

    • Verification Image

    • Background

    • Beschreibung

    Beschreibung

    8-OHdG (DNA/RNA Damage) Antibody is a Rabbit-derived and non-conjugated IgG polyclonal antibody, targeting to 8-OHdG (DNA/RNA Damage).

    Host

    Rabbit

    Clonality

    Polyclonal

    Molekulargewicht

    Predicted band size: 0.283kDa

    Species Reactivity
    Species independent
    SwissProt ID

    Gene ID
    Immunogen

    KLH conjugated 8-OHdG

    Application &
    Dilution Ratio
    Application Dilution Ratio
    ELISA
    ELISA: Enzyme Linked Immunosorbent Assay
    1:5000-10000
    IHC-P
    IHC-P: Immunohistochemistry-Paraffin
    1:100-500
    IHC-F
    IHC-F: Immunohistochemistry-Frozen
    1:100-500
    IF-Tissue
    IF-Tissue: Immunofluorescence-Tissue
    1:100-500
    mIHC
    mIHC: Multiplex Immunohistochemical
    1:500
    Sensitivity Endogenous Reinheit affinity purified
    Conjugation Non-conjugated Modification Unmodified
    Isotype IgG  
    Appearance

    Liquid

    Formulation

    Supplied in 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol or 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

    Storage & Stability

    Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.

    Versand

    Shipping with blue ice.

    Verification Image
    mIHC
    • Tyramide signaling amplification based immunofluorescence was performed on paraffin-embedded human Colon cancer‌ tissue using 8-OHdG antibody. Antigen retrieval was performed in EDTA buffer pH 9.0 (95 °C, 20 min) followed by cooling to RT. Then incubated with primary antibody (HY-P81140, 1:500 dilution) at room temperature for 60 minutes and HRP conjugated secondary antibody for 10 minutes. Fluorescence was then developed with Vari Fluor 532 TSA (200×)(HY-D1832). The tissues were counterstained with DAPI and mounted with Anti-fade mounting medium.

    • Tyramide signaling amplification based immunofluorescence was performed on paraffin-embedded human Colon cancer‌ tissue using 8-OHdG antibody. Antigen retrieval was performed in EDTA buffer pH 9.0 (95 °C, 20 min) followed by cooling to RT. Then incubated with primary antibody (HY-P81140, 1:500 dilution) at room temperature for 60 minutes and HRP conjugated secondary antibody for 10 minutes. Fluorescence was then developed with Vari Fluor 532 TSA (200×)(HY-D1832). The tissues were counterstained with DAPI and mounted with Anti-fade mounting medium.

    • Tyramide signaling amplification based immunofluorescence was performed on paraffin-embedded human Colon cancer‌ tissue using 8-OHdG antibody. Antigen retrieval was performed in EDTA buffer pH 9.0 (95 °C, 20 min) followed by cooling to RT. Then incubated with primary antibody (HY-P81140, 1:500 dilution) at room temperature for 60 minutes and HRP conjugated secondary antibody for 10 minutes. Fluorescence was then developed with Vari Fluor 532 TSA (200×)(HY-D1832). The tissues were counterstained with DAPI and mounted with Anti-fade mounting medium.

    • Tyramide signaling amplification based immunofluorescence was performed on paraffin-embedded human Gastric Cancer tissue using 8-OHdG antibody. Antigen retrieval was performed in EDTA buffer pH 9.0 (95 °C, 20 min) followed by cooling to RT. Then incubated with primary antibody (HY-P81140, 1:500 dilution) at room temperature for 60 minutes and HRP conjugated secondary antibody for 10 minutes. Fluorescence was then developed with Vari Fluor 532 TSA (200×)(HY-D1832). The tissues were counterstained with DAPI and mounted with Anti-fade mounting medium.

    • Tyramide signaling amplification based immunofluorescence was performed on paraffin-embedded human Gastric Cancer tissue using 8-OHdG antibody. Antigen retrieval was performed in EDTA buffer pH 9.0 (95 °C, 20 min) followed by cooling to RT. Then incubated with primary antibody (HY-P81140, 1:500 dilution) at room temperature for 60 minutes and HRP conjugated secondary antibody for 10 minutes. Fluorescence was then developed with Vari Fluor 532 TSA (200×)(HY-D1832). The tissues were counterstained with DAPI and mounted with Anti-fade mounting medium.

    • Tyramide signaling amplification based immunofluorescence was performed on paraffin-embedded human Gastric Cancer tissue using 8-OHdG antibody. Antigen retrieval was performed in EDTA buffer pH 9.0 (95 °C, 20 min) followed by cooling to RT. Then incubated with primary antibody (HY-P81140, 1:500 dilution) at room temperature for 60 minutes and HRP conjugated secondary antibody for 10 minutes. Fluorescence was then developed with Vari Fluor 532 TSA (200×)(HY-D1832). The tissues were counterstained with DAPI and mounted with Anti-fade mounting medium.

    Background
    Function:8-Hydroxy-2'-deoxyguanosine (8-OHdG) is a marker formed in DNA after oxidation; guanine, the most sensitive base to free radical attack in DNA, can be converted to various markers such as 8-hydroxyguanine, 8-hydroxyguanosine, and 8-OHdG after oxidation. Among them, the 8-OHdG adduct is one of the most abundant base modifications excreted in urine, and due to its easy collection, it is commonly used as a biomarker for oxidative DNA damage. It is also the main product of DNA damage and can be used as an important biomarker to evaluate oxidative stress induced by exogenous compounds. Chronic arsenic exposure leads to elevated levels of urinary 8-OHdG, triclosan (TCS) exposure significantly increases 8-OHdG levels in zebrafish brain tissue, and levels of 8-OHdG in mitochondrial DNA isolated from the parietal cortex of patients with Alzheimer’s disease (AD) are significantly higher than those of age-matched controls. Additionally, the presence of 8-OHdG in DNA (also known as 8-hydroxyguanosine in RNA) is a reliable marker of base modifications, as it is consistently detected after oxidative stress generated by various conditions.
    RRID
    Synonyms
    8-hydroxy-2'-deoxyguanosine; 2'-Deoxy-8-oxoguanosine; 7,8-Dihydro-8-oxo-2'-deoxyguanosine; 8-Oxo-7,8-dihydro-2'-deoxyguanosine; 8-Oxo-7,8-dihydrodeoxyguanosine; 2'-Deoxy-8-oxo-D-guanosine; 8-Oxo-7,8-dihydro-2μ-deoxyguanosine,8-Oxo-dG; 2'-Deoxy-8-hydroxyguanosine;
    Dokumentation

    8-OHdG (DNA/RNA Damage) Antibody Related Classifications

    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    Produktname:
    8-OHdG (DNA/RNA Damage) Antibody
    Art. -Nr.:
    HY-P81140
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