rabbit monoclonal anti phospho histone h2a x ser139  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal anti phospho histone h2a x ser139
    Overview of the impact of melatonin administration on key skin aging biomarkers. ↑ = increased, ↔ = no change, ↓ = decreased, compared to the vehicle. Mann–Whitney or Student’s t -test, * p < 0.5, ** p < 0.01.
    Rabbit Monoclonal Anti Phospho Histone H2a X Ser139, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal anti phospho histone h2a x ser139/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    1) Product Images from "Melatonin Exerts Prominent, Differential Epidermal and Dermal Anti-Aging Properties in Aged Human Eyelid Skin Ex Vivo"

    Article Title: Melatonin Exerts Prominent, Differential Epidermal and Dermal Anti-Aging Properties in Aged Human Eyelid Skin Ex Vivo

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms242115963

    Overview of the impact of melatonin administration on key skin aging biomarkers. ↑ = increased, ↔ = no change, ↓ = decreased, compared to the vehicle. Mann–Whitney or Student’s t -test, * p < 0.5, ** p < 0.01.
    Figure Legend Snippet: Overview of the impact of melatonin administration on key skin aging biomarkers. ↑ = increased, ↔ = no change, ↓ = decreased, compared to the vehicle. Mann–Whitney or Student’s t -test, * p < 0.5, ** p < 0.01.

    Techniques Used:

    List of antibodies and immunohistochemical staining treatments used in the study.
    Figure Legend Snippet: List of antibodies and immunohistochemical staining treatments used in the study.

    Techniques Used: Immunohistochemistry, Staining, Blocking Assay, Amplification, Avidin-Biotin Assay

    rabbit monoclonal anti phospho histone h2a x ser139  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc rabbit monoclonal anti phospho histone h2a x ser139
    KEY RESOURCES TABLE
    Rabbit Monoclonal Anti Phospho Histone H2a X Ser139, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal anti phospho histone h2a x ser139/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    1) Product Images from "Irreversible cell cycle exit associated with senescence is mediated by constitutive MYC degradation"

    Article Title: Irreversible cell cycle exit associated with senescence is mediated by constitutive MYC degradation

    Journal: Cell reports

    doi: 10.1016/j.celrep.2023.113079

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Recombinant, Luminex, Staining, shRNA, Software, Imaging

    rabbit monoclonal anti phospho histone h2a x ser139  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc rabbit monoclonal anti phospho histone h2a x ser139

    Rabbit Monoclonal Anti Phospho Histone H2a X Ser139, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal anti phospho histone h2a x ser139/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    rabbit monoclonal anti phospho histone h2a x ser139 - by Bioz Stars, 2023-12
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    1) Product Images from "WNK1 is required during male pachynema to sustain fertility"

    Article Title: WNK1 is required during male pachynema to sustain fertility

    Journal: iScience

    doi: 10.1016/j.isci.2023.107616


    Figure Legend Snippet:

    Techniques Used: Recombinant, In Situ, Software

    rabbit monoclonal anti phospho histone h2a x ser139  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc rabbit monoclonal anti phospho histone h2a x ser139
    Key Resources Table
    Rabbit Monoclonal Anti Phospho Histone H2a X Ser139, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal anti phospho histone h2a x ser139/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    1) Product Images from "SPARCLE , a p53-induced lncRNA, controls apoptosis after genotoxic stress by promoting PARP-1 cleavage"

    Article Title: SPARCLE , a p53-induced lncRNA, controls apoptosis after genotoxic stress by promoting PARP-1 cleavage

    Journal: Molecular cell

    doi: 10.1016/j.molcel.2022.01.001

    Key Resources Table
    Figure Legend Snippet: Key Resources Table

    Techniques Used: Recombinant, Binding Assay, Modification, Protease Inhibitor, Immunoprecipitation, Hybridization, Staining, Labeling, TUNEL Assay, Caspase-Glo Assay, PCR Cloning, Luciferase, Reporter Assay, Purification, Gel Extraction, Plasmid Preparation, Western Blot, Microscopy, Negative Control, Software, Imaging

    phospho histone h2a x ser139 20e3 rabbit mab  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc phospho histone h2a x ser139 20e3 rabbit mab
    The characteristics of bone marrow-derived macrophages (BMDM) from mgmt control (mgmt fl/fl ; LysM-Cre -/- ) or mgmt null (mgmt fl/fl ; LysM-Cre cre/- ) mice at 24 h after activation by lipopolysaccharide (LPS) as indicated by supernatant cell-free DNA ( A ), malondialdehyde (MDA; a reactive stress molecule) ( B ), and immunofluorescent stained for DNA break (phospho-histone <t>H2A.X;</t> green color) and actin filament (red color) in intensity score and representative pictures ( C , D ) are demonstrated. Triplicated independent experiments were performed. Mean ± SEM with the one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 vs mgmt control DMEM; *, p ˂ 0.05 between the indicated groups.
    Phospho Histone H2a X Ser139 20e3 Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Less Severe Polymicrobial Sepsis in Conditional mgmt -Deleted Mice Using LysM-Cre System, Impacts of DNA Methylation and MGMT Inhibitor in Sepsis"

    Article Title: Less Severe Polymicrobial Sepsis in Conditional mgmt -Deleted Mice Using LysM-Cre System, Impacts of DNA Methylation and MGMT Inhibitor in Sepsis

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms241210175

    The characteristics of bone marrow-derived macrophages (BMDM) from mgmt control (mgmt fl/fl ; LysM-Cre -/- ) or mgmt null (mgmt fl/fl ; LysM-Cre cre/- ) mice at 24 h after activation by lipopolysaccharide (LPS) as indicated by supernatant cell-free DNA ( A ), malondialdehyde (MDA; a reactive stress molecule) ( B ), and immunofluorescent stained for DNA break (phospho-histone H2A.X; green color) and actin filament (red color) in intensity score and representative pictures ( C , D ) are demonstrated. Triplicated independent experiments were performed. Mean ± SEM with the one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 vs mgmt control DMEM; *, p ˂ 0.05 between the indicated groups.
    Figure Legend Snippet: The characteristics of bone marrow-derived macrophages (BMDM) from mgmt control (mgmt fl/fl ; LysM-Cre -/- ) or mgmt null (mgmt fl/fl ; LysM-Cre cre/- ) mice at 24 h after activation by lipopolysaccharide (LPS) as indicated by supernatant cell-free DNA ( A ), malondialdehyde (MDA; a reactive stress molecule) ( B ), and immunofluorescent stained for DNA break (phospho-histone H2A.X; green color) and actin filament (red color) in intensity score and representative pictures ( C , D ) are demonstrated. Triplicated independent experiments were performed. Mean ± SEM with the one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 vs mgmt control DMEM; *, p ˂ 0.05 between the indicated groups.

    Techniques Used: Derivative Assay, Activation Assay, Staining

    rabbit monoclonal anti phospho histone h2a x ser139  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc rabbit monoclonal anti phospho histone h2a x ser139
    KEY RESOURCES TABLE
    Rabbit Monoclonal Anti Phospho Histone H2a X Ser139, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal anti phospho histone h2a x ser139/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit monoclonal anti phospho histone h2a x ser139 - by Bioz Stars, 2023-12
    86/100 stars

    Images

    1) Product Images from "HAPSTR1 localizes HUWE1 to the nucleus to limit stress signaling pathways"

    Article Title: HAPSTR1 localizes HUWE1 to the nucleus to limit stress signaling pathways

    Journal: Cell reports

    doi: 10.1016/j.celrep.2023.112496

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Recombinant, Protease Inhibitor, Western Blot, SYBR Green Assay, Conjugation Assay, Bicinchoninic Acid Protein Assay, Luciferase, Viability Assay, Knock-In, Expressing, Sequencing, Software

    phospho histone h2a x ser139 20e3 rabbit mab  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc phospho histone h2a x ser139 20e3 rabbit mab
    The schema of the experiments in bone marrow-derived macrophages from mgmt control ( mgmt fl/fl ; LysM-Cre −/− and mgmt null ( mgmt fl/fl ; LysM-Cre cre/− ) mice after activation by lipopolysaccharide (LPS) in a single protocol (N/LPS), which started with the culture media followed by LPS 24 h later or LPS tolerance (LPS/LPS) by the two sequential LPS stimulations, or control (N/N), using the culture media incubation only ( A ). The characteristics of macrophages under these protocols, as indicated by the expression of mgmt ( B ), cell viability using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) ( C ), reactive oxygen species with dihydroethidium stain (DHE) ( D ), supernatant cell-free DNA ( E ), the DNA damage score with the representative immunofluorescent pictures of phosphohistone <t>H2A.X</t> (a DNA break biomarker) ( F , G ), and the energy status of cells (extracellular flux analysis) ( H – K ). Independent triplicated experiments were performed. Mean ± SEM with one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 mgmt vs. control DMEM; *, p ˂ 0.05 between the indicated groups.
    Phospho Histone H2a X Ser139 20e3 Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho histone h2a x ser139 20e3 rabbit mab/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    phospho histone h2a x ser139 20e3 rabbit mab - by Bioz Stars, 2023-12
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    1) Product Images from "Less Severe Lipopolysaccharide-Induced Inflammation in Conditional mgmt -Deleted Mice with LysM-Cre System: The Loss of DNA Repair in Macrophages"

    Article Title: Less Severe Lipopolysaccharide-Induced Inflammation in Conditional mgmt -Deleted Mice with LysM-Cre System: The Loss of DNA Repair in Macrophages

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms241210139

    The schema of the experiments in bone marrow-derived macrophages from mgmt control ( mgmt fl/fl ; LysM-Cre −/− and mgmt null ( mgmt fl/fl ; LysM-Cre cre/− ) mice after activation by lipopolysaccharide (LPS) in a single protocol (N/LPS), which started with the culture media followed by LPS 24 h later or LPS tolerance (LPS/LPS) by the two sequential LPS stimulations, or control (N/N), using the culture media incubation only ( A ). The characteristics of macrophages under these protocols, as indicated by the expression of mgmt ( B ), cell viability using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) ( C ), reactive oxygen species with dihydroethidium stain (DHE) ( D ), supernatant cell-free DNA ( E ), the DNA damage score with the representative immunofluorescent pictures of phosphohistone H2A.X (a DNA break biomarker) ( F , G ), and the energy status of cells (extracellular flux analysis) ( H – K ). Independent triplicated experiments were performed. Mean ± SEM with one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 mgmt vs. control DMEM; *, p ˂ 0.05 between the indicated groups.
    Figure Legend Snippet: The schema of the experiments in bone marrow-derived macrophages from mgmt control ( mgmt fl/fl ; LysM-Cre −/− and mgmt null ( mgmt fl/fl ; LysM-Cre cre/− ) mice after activation by lipopolysaccharide (LPS) in a single protocol (N/LPS), which started with the culture media followed by LPS 24 h later or LPS tolerance (LPS/LPS) by the two sequential LPS stimulations, or control (N/N), using the culture media incubation only ( A ). The characteristics of macrophages under these protocols, as indicated by the expression of mgmt ( B ), cell viability using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) ( C ), reactive oxygen species with dihydroethidium stain (DHE) ( D ), supernatant cell-free DNA ( E ), the DNA damage score with the representative immunofluorescent pictures of phosphohistone H2A.X (a DNA break biomarker) ( F , G ), and the energy status of cells (extracellular flux analysis) ( H – K ). Independent triplicated experiments were performed. Mean ± SEM with one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 mgmt vs. control DMEM; *, p ˂ 0.05 between the indicated groups.

    Techniques Used: Derivative Assay, Activation Assay, Incubation, Expressing, Staining, Biomarker Assay

    rabbit monoclonal anti phospho histone h2a x ser139  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc rabbit monoclonal anti phospho histone h2a x ser139
    The DNA damage response is activated in TREX1 knockout-induced cellular senescence MEFs were derived from day 13.5 mouse embryos and cellular senescence was induced by serial cell passaging. (A) Expression of <t>γ-H2AX</t> protein, a marker of DNA damage, detected by immunoblot in passage 8 of MEFs. (B) Quantitative analysis of (A); GAPDH was used as control (n = 3 biological replicates). (C and D) Nuclear DNA damage in passage 8 MEFs detected by immunofluorescence (γ-H2AX [red], H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]), (D) Quantitative analysis of nuclear DNA damage positive cell (n = 3 biological replicates). (E and F) Micronuclei distribution in passage 8 Trex1 −/− MEFs detected by immunofluorescence (dsDNA [red], γ-H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]); zoom shows an enlarged region of dsDNA, γ-H2AX, and DAPI co-localization in the cytoplasm, (F) Quantitative analysis of Micronuclei positive cell (n = 3 biological replicates). (G) Expression of DDR and cellular senescence marker proteins at passage 8 MEFs by immunoblotting. (H) Quantitative analysis of p-RB, p -Chk2, and p16 proteins, with GAPDH as control (n = 3 biological replicates). (I and J) In passages 8, WT, Trex1 −/− MEFs cell cycle was assessed by FACS (n = 3 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values were calculated using by one-way ANOVA versus WT with Dunnett’s correction (B, C, F, H, J). For gel source data, see Mendeley Data.
    Rabbit Monoclonal Anti Phospho Histone H2a X Ser139, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal anti phospho histone h2a x ser139/product/Cell Signaling Technology Inc
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    rabbit monoclonal anti phospho histone h2a x ser139 - by Bioz Stars, 2023-12
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    1) Product Images from "Suppression of TREX1 deficiency-induced cellular senescence and interferonopathies by inhibition of DNA damage response"

    Article Title: Suppression of TREX1 deficiency-induced cellular senescence and interferonopathies by inhibition of DNA damage response

    Journal: iScience

    doi: 10.1016/j.isci.2023.107090

    The DNA damage response is activated in TREX1 knockout-induced cellular senescence MEFs were derived from day 13.5 mouse embryos and cellular senescence was induced by serial cell passaging. (A) Expression of γ-H2AX protein, a marker of DNA damage, detected by immunoblot in passage 8 of MEFs. (B) Quantitative analysis of (A); GAPDH was used as control (n = 3 biological replicates). (C and D) Nuclear DNA damage in passage 8 MEFs detected by immunofluorescence (γ-H2AX [red], H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]), (D) Quantitative analysis of nuclear DNA damage positive cell (n = 3 biological replicates). (E and F) Micronuclei distribution in passage 8 Trex1 −/− MEFs detected by immunofluorescence (dsDNA [red], γ-H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]); zoom shows an enlarged region of dsDNA, γ-H2AX, and DAPI co-localization in the cytoplasm, (F) Quantitative analysis of Micronuclei positive cell (n = 3 biological replicates). (G) Expression of DDR and cellular senescence marker proteins at passage 8 MEFs by immunoblotting. (H) Quantitative analysis of p-RB, p -Chk2, and p16 proteins, with GAPDH as control (n = 3 biological replicates). (I and J) In passages 8, WT, Trex1 −/− MEFs cell cycle was assessed by FACS (n = 3 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values were calculated using by one-way ANOVA versus WT with Dunnett’s correction (B, C, F, H, J). For gel source data, see Mendeley Data.
    Figure Legend Snippet: The DNA damage response is activated in TREX1 knockout-induced cellular senescence MEFs were derived from day 13.5 mouse embryos and cellular senescence was induced by serial cell passaging. (A) Expression of γ-H2AX protein, a marker of DNA damage, detected by immunoblot in passage 8 of MEFs. (B) Quantitative analysis of (A); GAPDH was used as control (n = 3 biological replicates). (C and D) Nuclear DNA damage in passage 8 MEFs detected by immunofluorescence (γ-H2AX [red], H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]), (D) Quantitative analysis of nuclear DNA damage positive cell (n = 3 biological replicates). (E and F) Micronuclei distribution in passage 8 Trex1 −/− MEFs detected by immunofluorescence (dsDNA [red], γ-H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]); zoom shows an enlarged region of dsDNA, γ-H2AX, and DAPI co-localization in the cytoplasm, (F) Quantitative analysis of Micronuclei positive cell (n = 3 biological replicates). (G) Expression of DDR and cellular senescence marker proteins at passage 8 MEFs by immunoblotting. (H) Quantitative analysis of p-RB, p -Chk2, and p16 proteins, with GAPDH as control (n = 3 biological replicates). (I and J) In passages 8, WT, Trex1 −/− MEFs cell cycle was assessed by FACS (n = 3 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values were calculated using by one-way ANOVA versus WT with Dunnett’s correction (B, C, F, H, J). For gel source data, see Mendeley Data.

    Techniques Used: Knock-Out, Derivative Assay, Passaging, Expressing, Marker, Western Blot, Immunofluorescence

    TREX1 knockout exacerbates IR-induced cellular senescence in MEFs Cellular senescence was induced by IR in 1 or 2 passage MEFs derived from E13.5 mouse embryos. (A) In 1 or 2 passage MEFs were pre-treated with 6 Gy IR for 6 days, then subjected to SA-β-Gal analysis. (B) Histograms indicate the percentages of SA-β-gal-positive cells (n = 3 biological replicates). (C–G) Expression level of SASP factors examined by RT-qPCR (n = 3 biological replicates). (H) Micronuclei distribution of Trex1 −/− MEFs were pre-treated with 6 Gy IR detected by immunofluorescence (dsDNA [red], γ-H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]); zoom shows an enlarged region of dsDNA, γ-H2AX, and DAPI co-localization in the cytoplasm. (I) Expression of DDR and cellular senescence marker proteins measured by immunoblotting. (J) Quantitative analysis of p-RB, p -CHK2, p21, and γ-H2AX proteins, with GAPDH as control (n = 3 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values calculated using two-way ANOVA with Bonferroni’s correction (B-G, J). For gel source data, see Mendeley Data.
    Figure Legend Snippet: TREX1 knockout exacerbates IR-induced cellular senescence in MEFs Cellular senescence was induced by IR in 1 or 2 passage MEFs derived from E13.5 mouse embryos. (A) In 1 or 2 passage MEFs were pre-treated with 6 Gy IR for 6 days, then subjected to SA-β-Gal analysis. (B) Histograms indicate the percentages of SA-β-gal-positive cells (n = 3 biological replicates). (C–G) Expression level of SASP factors examined by RT-qPCR (n = 3 biological replicates). (H) Micronuclei distribution of Trex1 −/− MEFs were pre-treated with 6 Gy IR detected by immunofluorescence (dsDNA [red], γ-H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]); zoom shows an enlarged region of dsDNA, γ-H2AX, and DAPI co-localization in the cytoplasm. (I) Expression of DDR and cellular senescence marker proteins measured by immunoblotting. (J) Quantitative analysis of p-RB, p -CHK2, p21, and γ-H2AX proteins, with GAPDH as control (n = 3 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values calculated using two-way ANOVA with Bonferroni’s correction (B-G, J). For gel source data, see Mendeley Data.

    Techniques Used: Knock-Out, Derivative Assay, Expressing, Quantitative RT-PCR, Immunofluorescence, Marker, Western Blot

    Activation of the cGAS-STING pathway is essential for TREX1 knockout-induced cellular senescence MEFs were derived from E13.5 mouse embryos. (A)Proliferation curve of primary WT, Trex1 −/− , cGas −/− , and Trex1 −/− cGas −/− MEFs cultured under 20% O2. B) Cellular senescence of WT, Trex1 −/− , cGas −/− , Trex1 −/− cGas −/− MFEs in 8 passages was analyzed by SA-β-Gal staining. C) Histograms indicate the percentage of SA-β-gal-positive cells (n = 3 biological replicates). (D) WT, Trex1 −/− , cGas −/− , Trex1 −/− cGas −/− MFEs in 10 passages expression of depicted genes was measured via RT-qPCR (n = 3 biological replicates). (E) ROS levels in WT, Trex1 −/− , cGas −/− , Trex1 −/− cGas −/− MFEs cells in 8 passages detected by flow cytometry. (F) Statistical results of flow cytometry (n = 3 biological replicates). (G) Expression of DDR and cellular senescence marker proteins measured by immunoblotting. (H) Quantitative analysis of p-RB, p -CHK2, p-p53, p21, and γ-H2AX proteins, with GAPDH as control (n = 3 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values were calculated using by one-way ANOVA versus WT with Dunnett’s correction (C, D, F, H). For gel source data, see Mendeley Data.
    Figure Legend Snippet: Activation of the cGAS-STING pathway is essential for TREX1 knockout-induced cellular senescence MEFs were derived from E13.5 mouse embryos. (A)Proliferation curve of primary WT, Trex1 −/− , cGas −/− , and Trex1 −/− cGas −/− MEFs cultured under 20% O2. B) Cellular senescence of WT, Trex1 −/− , cGas −/− , Trex1 −/− cGas −/− MFEs in 8 passages was analyzed by SA-β-Gal staining. C) Histograms indicate the percentage of SA-β-gal-positive cells (n = 3 biological replicates). (D) WT, Trex1 −/− , cGas −/− , Trex1 −/− cGas −/− MFEs in 10 passages expression of depicted genes was measured via RT-qPCR (n = 3 biological replicates). (E) ROS levels in WT, Trex1 −/− , cGas −/− , Trex1 −/− cGas −/− MFEs cells in 8 passages detected by flow cytometry. (F) Statistical results of flow cytometry (n = 3 biological replicates). (G) Expression of DDR and cellular senescence marker proteins measured by immunoblotting. (H) Quantitative analysis of p-RB, p -CHK2, p-p53, p21, and γ-H2AX proteins, with GAPDH as control (n = 3 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values were calculated using by one-way ANOVA versus WT with Dunnett’s correction (C, D, F, H). For gel source data, see Mendeley Data.

    Techniques Used: Activation Assay, Knock-Out, Derivative Assay, Cell Culture, Staining, Expressing, Quantitative RT-PCR, Flow Cytometry, Marker, Western Blot

    Cellular senescence in Trex1 knockout lupus-like mice 4 - 5-month-old WT and Trex1 −/− lupus-like mice were compared. (A and B) Heart (A) and liver (B) fibrosis were examined by Sirius red staining. (C) Representative images of SA-β-gal staining on kidney from WT, Trex1 −/− mouse. (D) Immunohistochemistry representative images of p21 on kidney from WT, Trex1 −/− mouse. (E and F) Representative images of γ-H2AX and p16 in sit hybridization with immunofluorescence of kidney, (F) Quantitative analysis of γ-H2AX and p16 positive cell (n = 3 biological replicates). (G) Expression of p -CHK2, p53, p21 and γ-H2AX in the heart was measured by immunoblotting. (H) Quantitative analysis of p -CHK2, p53, p21 and γ-H2AX with GAPDH as control (n = 3 biological replicates). (I and J) mRNA expression of IFNβ, ISGs, SASP factors, and aging marker proteins in the heart by RT-qPCR (n > 6 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values were calculated using by one-way ANOVA versus WT with Dunnett’s correction (A–D, F, H–J).
    Figure Legend Snippet: Cellular senescence in Trex1 knockout lupus-like mice 4 - 5-month-old WT and Trex1 −/− lupus-like mice were compared. (A and B) Heart (A) and liver (B) fibrosis were examined by Sirius red staining. (C) Representative images of SA-β-gal staining on kidney from WT, Trex1 −/− mouse. (D) Immunohistochemistry representative images of p21 on kidney from WT, Trex1 −/− mouse. (E and F) Representative images of γ-H2AX and p16 in sit hybridization with immunofluorescence of kidney, (F) Quantitative analysis of γ-H2AX and p16 positive cell (n = 3 biological replicates). (G) Expression of p -CHK2, p53, p21 and γ-H2AX in the heart was measured by immunoblotting. (H) Quantitative analysis of p -CHK2, p53, p21 and γ-H2AX with GAPDH as control (n = 3 biological replicates). (I and J) mRNA expression of IFNβ, ISGs, SASP factors, and aging marker proteins in the heart by RT-qPCR (n > 6 biological replicates). Data represent mean ± S.E.M. of at least 3 independent experiments. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001, p values were calculated using by one-way ANOVA versus WT with Dunnett’s correction (A–D, F, H–J).

    Techniques Used: Knock-Out, Staining, Immunohistochemistry, Hybridization, Immunofluorescence, Expressing, Western Blot, Marker, Quantitative RT-PCR


    Figure Legend Snippet:

    Techniques Used: Recombinant, Protein Extraction, CCK-8 Assay, Enzyme-linked Immunosorbent Assay, Bicinchoninic Acid Protein Assay, Software

    phospho histone h2a x ser139 20e3 rabbit mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho histone h2a x ser139 20e3 rabbit mab
    DFO treatment of HepG2 cells induces either apoptosis or extensive morphological modifications, with the surviving cells losing their 3D structure and undergoing cell cycle arrest and DNA damage. (A) Representative pictures of HepG2 cells before and after DFO treatment acquired with an optical microscope (scale bar = 100 µm) and a confocal microscope after staining with DAPI (3D visualization; scale bar = 50 µm). Enlarged cells after 7 days of DFO treatment are delineated with a discontinuous black line; red arrows indicate apoptotic cells. (B) Protein expression levels of PARP, yH2AX, and survivin in untreated and treated HepG2 cells determined by immunoblotting. Graphs representing the immunoblots bands quantification are shown in Supplementary File 2, . (C) Cell cycle analysis of untreated, 72 h DFO-treated, and 7-day DFO-treated HepG2 cells. (D) Representative images of control and 7-day DFO-treated HepG2 cells stained for <t>phospho-H2AX</t> foci (green) and DAPI (blue). Cells were observed and imaged using a confocal microscope. Scale bar = 25 µm.
    Phospho Histone H2a X Ser139 20e3 Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Reduced sulfatide content in deferoxamine-induced senescent HepG2 cells"

    Article Title: Reduced sulfatide content in deferoxamine-induced senescent HepG2 cells

    Journal: The International Journal of Biochemistry & Cell Biology

    doi: 10.1016/j.biocel.2023.106419

    DFO treatment of HepG2 cells induces either apoptosis or extensive morphological modifications, with the surviving cells losing their 3D structure and undergoing cell cycle arrest and DNA damage. (A) Representative pictures of HepG2 cells before and after DFO treatment acquired with an optical microscope (scale bar = 100 µm) and a confocal microscope after staining with DAPI (3D visualization; scale bar = 50 µm). Enlarged cells after 7 days of DFO treatment are delineated with a discontinuous black line; red arrows indicate apoptotic cells. (B) Protein expression levels of PARP, yH2AX, and survivin in untreated and treated HepG2 cells determined by immunoblotting. Graphs representing the immunoblots bands quantification are shown in Supplementary File 2, . (C) Cell cycle analysis of untreated, 72 h DFO-treated, and 7-day DFO-treated HepG2 cells. (D) Representative images of control and 7-day DFO-treated HepG2 cells stained for phospho-H2AX foci (green) and DAPI (blue). Cells were observed and imaged using a confocal microscope. Scale bar = 25 µm.
    Figure Legend Snippet: DFO treatment of HepG2 cells induces either apoptosis or extensive morphological modifications, with the surviving cells losing their 3D structure and undergoing cell cycle arrest and DNA damage. (A) Representative pictures of HepG2 cells before and after DFO treatment acquired with an optical microscope (scale bar = 100 µm) and a confocal microscope after staining with DAPI (3D visualization; scale bar = 50 µm). Enlarged cells after 7 days of DFO treatment are delineated with a discontinuous black line; red arrows indicate apoptotic cells. (B) Protein expression levels of PARP, yH2AX, and survivin in untreated and treated HepG2 cells determined by immunoblotting. Graphs representing the immunoblots bands quantification are shown in Supplementary File 2, . (C) Cell cycle analysis of untreated, 72 h DFO-treated, and 7-day DFO-treated HepG2 cells. (D) Representative images of control and 7-day DFO-treated HepG2 cells stained for phospho-H2AX foci (green) and DAPI (blue). Cells were observed and imaged using a confocal microscope. Scale bar = 25 µm.

    Techniques Used: Microscopy, Staining, Expressing, Western Blot, Cell Cycle Assay

    antibody γh2ax  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc antibody γh2ax
    (A) N2A cells were treated with camptothecin (CPT) or PBS (Control), fixed, and analyzed by immunofluorescence using an antibody that detects the DNA damage marker, <t>γH2AX.</t> (B) The Input and immunoprecipitated samples from nuclear fractions (Bound) treated with either CPT or PBS (Control) for both EXOSC3 and control IgG (Ctrl IgG) are shown. DDX1, EXOSC9, and EXOSC3 are detected. (C) The immunoprecipitation experiment in was performed in biological triplicate and DDX1 bands in EXOSC3 Bound fractions were quantified. Statistical significance was calculated by a student’s T-test. Asterisk (*) represents p-value < 0.05. IP: immunoprecipitation; IB: immunoblot.
    Antibody γh2ax, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/antibody γh2ax/product/Cell Signaling Technology Inc
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    antibody γh2ax - by Bioz Stars, 2023-12
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    Images

    1) Product Images from "The RNA helicase DDX1 associates with the nuclear RNA exosome and modulates R-loops"

    Article Title: The RNA helicase DDX1 associates with the nuclear RNA exosome and modulates R-loops

    Journal: bioRxiv

    doi: 10.1101/2023.04.17.537228

    (A) N2A cells were treated with camptothecin (CPT) or PBS (Control), fixed, and analyzed by immunofluorescence using an antibody that detects the DNA damage marker, γH2AX. (B) The Input and immunoprecipitated samples from nuclear fractions (Bound) treated with either CPT or PBS (Control) for both EXOSC3 and control IgG (Ctrl IgG) are shown. DDX1, EXOSC9, and EXOSC3 are detected. (C) The immunoprecipitation experiment in was performed in biological triplicate and DDX1 bands in EXOSC3 Bound fractions were quantified. Statistical significance was calculated by a student’s T-test. Asterisk (*) represents p-value < 0.05. IP: immunoprecipitation; IB: immunoblot.
    Figure Legend Snippet: (A) N2A cells were treated with camptothecin (CPT) or PBS (Control), fixed, and analyzed by immunofluorescence using an antibody that detects the DNA damage marker, γH2AX. (B) The Input and immunoprecipitated samples from nuclear fractions (Bound) treated with either CPT or PBS (Control) for both EXOSC3 and control IgG (Ctrl IgG) are shown. DDX1, EXOSC9, and EXOSC3 are detected. (C) The immunoprecipitation experiment in was performed in biological triplicate and DDX1 bands in EXOSC3 Bound fractions were quantified. Statistical significance was calculated by a student’s T-test. Asterisk (*) represents p-value < 0.05. IP: immunoprecipitation; IB: immunoblot.

    Techniques Used: Immunofluorescence, Marker, Immunoprecipitation, Western Blot

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    Cell Signaling Technology Inc rabbit monoclonal anti phospho histone h2a x ser139
    Overview of the impact of melatonin administration on key skin aging biomarkers. ↑ = increased, ↔ = no change, ↓ = decreased, compared to the vehicle. Mann–Whitney or Student’s t -test, * p < 0.5, ** p < 0.01.
    Rabbit Monoclonal Anti Phospho Histone H2a X Ser139, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal anti phospho histone h2a x ser139/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc phospho histone h2a x ser139 20e3 rabbit mab
    The characteristics of bone marrow-derived macrophages (BMDM) from mgmt control (mgmt fl/fl ; LysM-Cre -/- ) or mgmt null (mgmt fl/fl ; LysM-Cre cre/- ) mice at 24 h after activation by lipopolysaccharide (LPS) as indicated by supernatant cell-free DNA ( A ), malondialdehyde (MDA; a reactive stress molecule) ( B ), and immunofluorescent stained for DNA break (phospho-histone <t>H2A.X;</t> green color) and actin filament (red color) in intensity score and representative pictures ( C , D ) are demonstrated. Triplicated independent experiments were performed. Mean ± SEM with the one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 vs mgmt control DMEM; *, p ˂ 0.05 between the indicated groups.
    Phospho Histone H2a X Ser139 20e3 Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho histone h2a x ser139 20e3 rabbit mab/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc antibody γh2ax
    (A) N2A cells were treated with camptothecin (CPT) or PBS (Control), fixed, and analyzed by immunofluorescence using an antibody that detects the DNA damage marker, <t>γH2AX.</t> (B) The Input and immunoprecipitated samples from nuclear fractions (Bound) treated with either CPT or PBS (Control) for both EXOSC3 and control IgG (Ctrl IgG) are shown. DDX1, EXOSC9, and EXOSC3 are detected. (C) The immunoprecipitation experiment in was performed in biological triplicate and DDX1 bands in EXOSC3 Bound fractions were quantified. Statistical significance was calculated by a student’s T-test. Asterisk (*) represents p-value < 0.05. IP: immunoprecipitation; IB: immunoblot.
    Antibody γh2ax, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/antibody γh2ax/product/Cell Signaling Technology Inc
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    Image Search Results


    Overview of the impact of melatonin administration on key skin aging biomarkers. ↑ = increased, ↔ = no change, ↓ = decreased, compared to the vehicle. Mann–Whitney or Student’s t -test, * p < 0.5, ** p < 0.01.

    Journal: International Journal of Molecular Sciences

    Article Title: Melatonin Exerts Prominent, Differential Epidermal and Dermal Anti-Aging Properties in Aged Human Eyelid Skin Ex Vivo

    doi: 10.3390/ijms242115963

    Figure Lengend Snippet: Overview of the impact of melatonin administration on key skin aging biomarkers. ↑ = increased, ↔ = no change, ↓ = decreased, compared to the vehicle. Mann–Whitney or Student’s t -test, * p < 0.5, ** p < 0.01.

    Article Snippet: , γH2A.x , 4% PFA, 10 min at RT , 10% goat serum in PBS , rabbit monoclonal anti-phospho-histone H2A.X (Ser139) (γH2A.X) (1:1500; Cell Signaling, #2577S) , goat monoclonal anti-rabbit IgG-Alexa Fluor 555 (1:400; Invitrogen, A21428).

    Techniques:

    List of antibodies and immunohistochemical staining treatments used in the study.

    Journal: International Journal of Molecular Sciences

    Article Title: Melatonin Exerts Prominent, Differential Epidermal and Dermal Anti-Aging Properties in Aged Human Eyelid Skin Ex Vivo

    doi: 10.3390/ijms242115963

    Figure Lengend Snippet: List of antibodies and immunohistochemical staining treatments used in the study.

    Article Snippet: , γH2A.x , 4% PFA, 10 min at RT , 10% goat serum in PBS , rabbit monoclonal anti-phospho-histone H2A.X (Ser139) (γH2A.X) (1:1500; Cell Signaling, #2577S) , goat monoclonal anti-rabbit IgG-Alexa Fluor 555 (1:400; Invitrogen, A21428).

    Techniques: Immunohistochemistry, Staining, Blocking Assay, Amplification, Avidin-Biotin Assay

    The characteristics of bone marrow-derived macrophages (BMDM) from mgmt control (mgmt fl/fl ; LysM-Cre -/- ) or mgmt null (mgmt fl/fl ; LysM-Cre cre/- ) mice at 24 h after activation by lipopolysaccharide (LPS) as indicated by supernatant cell-free DNA ( A ), malondialdehyde (MDA; a reactive stress molecule) ( B ), and immunofluorescent stained for DNA break (phospho-histone H2A.X; green color) and actin filament (red color) in intensity score and representative pictures ( C , D ) are demonstrated. Triplicated independent experiments were performed. Mean ± SEM with the one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 vs mgmt control DMEM; *, p ˂ 0.05 between the indicated groups.

    Journal: International Journal of Molecular Sciences

    Article Title: Less Severe Polymicrobial Sepsis in Conditional mgmt -Deleted Mice Using LysM-Cre System, Impacts of DNA Methylation and MGMT Inhibitor in Sepsis

    doi: 10.3390/ijms241210175

    Figure Lengend Snippet: The characteristics of bone marrow-derived macrophages (BMDM) from mgmt control (mgmt fl/fl ; LysM-Cre -/- ) or mgmt null (mgmt fl/fl ; LysM-Cre cre/- ) mice at 24 h after activation by lipopolysaccharide (LPS) as indicated by supernatant cell-free DNA ( A ), malondialdehyde (MDA; a reactive stress molecule) ( B ), and immunofluorescent stained for DNA break (phospho-histone H2A.X; green color) and actin filament (red color) in intensity score and representative pictures ( C , D ) are demonstrated. Triplicated independent experiments were performed. Mean ± SEM with the one-way ANOVA followed by Tukey’s analysis was used. #, p ˂ 0.05 vs mgmt control DMEM; *, p ˂ 0.05 between the indicated groups.

    Article Snippet: Fixed samples were blocked with 2% bovine serum albumin in 1X TBS for 1 h at room temperature and then incubated overnight at 4 °C with phospho-histone H2A.X (Ser139) (20E3) rabbit mAb (Cell signaling).

    Techniques: Derivative Assay, Activation Assay, Staining

    (A) N2A cells were treated with camptothecin (CPT) or PBS (Control), fixed, and analyzed by immunofluorescence using an antibody that detects the DNA damage marker, γH2AX. (B) The Input and immunoprecipitated samples from nuclear fractions (Bound) treated with either CPT or PBS (Control) for both EXOSC3 and control IgG (Ctrl IgG) are shown. DDX1, EXOSC9, and EXOSC3 are detected. (C) The immunoprecipitation experiment in was performed in biological triplicate and DDX1 bands in EXOSC3 Bound fractions were quantified. Statistical significance was calculated by a student’s T-test. Asterisk (*) represents p-value < 0.05. IP: immunoprecipitation; IB: immunoblot.

    Journal: bioRxiv

    Article Title: The RNA helicase DDX1 associates with the nuclear RNA exosome and modulates R-loops

    doi: 10.1101/2023.04.17.537228

    Figure Lengend Snippet: (A) N2A cells were treated with camptothecin (CPT) or PBS (Control), fixed, and analyzed by immunofluorescence using an antibody that detects the DNA damage marker, γH2AX. (B) The Input and immunoprecipitated samples from nuclear fractions (Bound) treated with either CPT or PBS (Control) for both EXOSC3 and control IgG (Ctrl IgG) are shown. DDX1, EXOSC9, and EXOSC3 are detected. (C) The immunoprecipitation experiment in was performed in biological triplicate and DDX1 bands in EXOSC3 Bound fractions were quantified. Statistical significance was calculated by a student’s T-test. Asterisk (*) represents p-value < 0.05. IP: immunoprecipitation; IB: immunoblot.

    Article Snippet: Coverslips were then blocked with 5% BSA for 60 minutes at room temperature and incubated overnight at 4°C with primary antibody γH2AX (rabbit monoclonal; Cell Signaling 9718T, 1:400).

    Techniques: Immunofluorescence, Marker, Immunoprecipitation, Western Blot