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hydroxy guanine 8 ohdg  (Novus Biologicals)


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    Structured Review

    Novus Biologicals hydroxy guanine 8 ohdg
    ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of <t>8-OHdG</t> ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .
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    Images

    1) Product Images from "Metabolic rewiring of macrophages by epidermal-derived lactate promotes sterile inflammation in the murine skin"

    Article Title: Metabolic rewiring of macrophages by epidermal-derived lactate promotes sterile inflammation in the murine skin

    Journal: The EMBO Journal

    doi: 10.1038/s44318-024-00039-y

    ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of 8-OHdG ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .
    Figure Legend Snippet: ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of 8-OHdG ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .

    Techniques Used: Immunostaining, Expressing, Control, Microscopy, Software, Quantitative Proteomics

    Table showing details of all antibodies used for the manuscript.
    Figure Legend Snippet: Table showing details of all antibodies used for the manuscript.

    Techniques Used:



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    ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of <t>8-OHdG</t> ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .
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    ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of <t>8-OHdG</t> ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .
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    ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of <t>8-OHdG</t> ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .
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    ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of <t>8-OHdG</t> ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .
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    Image Search Results


    ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of 8-OHdG ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .

    Journal: The EMBO Journal

    Article Title: Metabolic rewiring of macrophages by epidermal-derived lactate promotes sterile inflammation in the murine skin

    doi: 10.1038/s44318-024-00039-y

    Figure Lengend Snippet: ( A ) ROS-associated pathways upregulated in GSEA analysis of epidermal compartment in E18.5 cKO skin compared to controls ( A ). ( B ) IF immunostaining of cKO skin showing the expression of 8-OHdG ( G ) in E16.5 KO and control skin ( N = 3). ( C ) Quantification of temporal change in the expression of 8-OHdG expression in cKO and control skin ( N ≥ 3). ( D ) qPCR showing increased transcription of genes associated with ROS generation in the cKO epidermis compared to WT ( N ≥ 3). ( E ) qPCR showing increased transcription of genes associated with ROS scavenging in the cKO epidermis compared to WT ( N ≥ 3). ( F ) IF showing increased expression of Catalase and Glutathione in cKO skin compared to WT ( N = 3). ( G ) cKO skin showing reduced expression of 8-OHdG and HIF1α after treatment with NAC compared to controls ( N = 4). ( H ) cKO skin showing reduced expression of GLUT1 and LDHa quantified in ( J ) in NAC, treated cKO skin compared to controls ( N = 3). ( I ) Quantification for ( G ) ( N = 4). ( J ) Quantification for ( H ) ( N = 3). ( K ) Schematic showing ROS-mediated regulation of HIF1α in cKO skin. Data Information: All the microscope images ( B , F , G , H ) were quantified ( C , I , J ) in ImageJ software. The number of biological replicates ( N ) for each panel is given in the figure legend. Scale bars: 50 μm. Student’s t-test was performed for statistical analysis. * p ≤ 0.05, * *p ≤ 0.01, **** p ≤ 0.0001, ns = not significant (student’s t test). All graphs are presented as mean ± SEM. WT experimental values are normalized to 1 for relative quantification. .

    Article Snippet: 12. , 8 hydroxy guanine (8-OHdG) , Novus Biologicals , NB100-1508 , 1:200.

    Techniques: Immunostaining, Expressing, Control, Microscopy, Software, Quantitative Proteomics

    Table showing details of all antibodies used for the manuscript.

    Journal: The EMBO Journal

    Article Title: Metabolic rewiring of macrophages by epidermal-derived lactate promotes sterile inflammation in the murine skin

    doi: 10.1038/s44318-024-00039-y

    Figure Lengend Snippet: Table showing details of all antibodies used for the manuscript.

    Article Snippet: 12. , 8 hydroxy guanine (8-OHdG) , Novus Biologicals , NB100-1508 , 1:200.

    Techniques: