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

Structured Review

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
Images
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

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:

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)

Structured Review

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
Images
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

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)

Structured Review

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
Images
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)

Structured Review

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
Images
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

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)

Structured Review

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
Price from $9.99 to $1999.99
Images
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

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)

Structured Review

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
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

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)

Structured Review

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
Price from $9.99 to $1999.99
Images
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

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)

Structured Review
![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.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_0204/pmc10320204/pmc10320204__gr2.jpg)
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
Images
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
![... induced by serial cell passaging. (A) Expression of γ-H2AX protein, a marker of DNA damage, detected by ... 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.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_0204/pmc10320204/pmc10320204__gr2.jpg)
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
![... 6 Gy IR detected by immunofluorescence (dsDNA [red], γ-H2AX [green], 4,6-diamididine-2-phenylindole (DAPI) [blue]); zoom shows an enlarged ... 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.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_0204/pmc10320204/pmc10320204__gr3.jpg)
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

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

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)

Structured Review

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
Price from $9.99 to $1999.99
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

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)

Structured Review

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
Average 98 stars, based on 1 article reviews
Price from $9.99 to $1999.99
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

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