Histone H3 [Citrulline Arg17, Citrulline Arg2, Citrulline Arg8] Antibody
Novus Biologicals | Catalog # NB100-57135
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Theoretical MW
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images
Immunocytochemistry/ Immunofluorescence: Histone H3 [Citrulline Arg17, Citrulline Arg2, Citrulline Arg8] Antibody [NB100-57135]
Immunocytochemistry/Immunofluorescence: Histone H3 [Citrulline 2, Citrulline 8, Citrulline 17] Antibody [NB100-57135] - HL60 cells treated with DMSO and Calcimycin Green: (at 1:1000 Blue Hoechst)Western Blot: Histone H3 [Citrulline Arg17, Citrulline Arg2, Citrulline Arg8] Antibody [NB100-57135]
Western Blot: Histone H3 [Citrulline 2, Citrulline 8, Citrulline 17] Antibody [NB100-57135] - Histone H3/Citrulline (R2,R8,R17) at 1:10000 dilution. Observed molecular weight is ~15 kDa.Immunohistochemistry: Rabbit Polyclonal Histone H3 [Citrulline Arg17, Citrulline Arg2, Citrulline Arg8] Antibody [NB100-57135]
Immunohistochemistry: Rabbit Polyclonal Histone H3 [Citrulline Arg17, Citrulline Arg2, Citrulline Arg8] Antibody [NB100-57135] - Analysis of Histone H3 on mouse brain tissue. Nucleus (Blue, DAPI) ; H3cit (green). Hemorrhagic stroke model FxFr ; 10 µm thickness 1:400 Secondary antibody AF488. Image from a verified customer review.Immunocytochemistry/ Immunofluorescence: Histone H3 [Citrulline Arg17, Citrulline Arg2, Citrulline Arg8] Antibody [NB100-57135] -
CLEC2.Fc inhibits SARS‐CoV‐2‐induced immunothrombosis in lungAAAV‐hACE2 mice were treated with saline and challenged with SARS‐CoV‐2 (8 × 104 PFU) for 5 days. Lung tissue sections were stained with DAPI (blue), anti‐MPO antibody (green), anti‐citrullinated histone H3 (Cit‐H3) antibody (red), anti‐CD42b antibody (yellow) and anti‐CD31 antibody (gray). yellow arrow: NETs (DNA+Gr‐1+MPO+Cit‐H3+); red arrow: immunothrombosis (NETs + thrombus (CD42b+)), Scale bar is 100 μm.B, CFor prophylactic treatment, CLEC2.Fc (or vehicle) was given at 1 h before virus challenge; for therapeutic treatment, CLEC2.Fc was given at 8 h post‐infection. The area of NET (colocalization area of MPO and Cit‐H3) (B) and immunothrombosis (colocalization area of Cit‐H3 and CD42b) (C) were measured using MetaMorph software.Data information: Data are mean +/- SEM from two independent experiments (saline: n = 3 for 3 d.p.i., n = 4 for 5 d.p.i.; isotype: n = 3 for 3 d.p.i., n = 4 for 5 d.p.i.; prophylactic treatment of CLEC2.Fc treatment: n = 5 for 3 d.p.i. and 5 d.p.i.; therapeutic treatment of CLEC2.Fc: n = 3 for 3 d.p.i. and 5 d.p.i.). *P < 0.05, **P < 0.01 (two‐way ANOVA).Source data are available online for this figure. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37211986), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications
Chromatin Immunoprecipitation (ChIP)
Immunocytochemistry/ Immunofluorescence
Immunohistochemistry
Immunohistochemistry-Paraffin
Western Blot
Reviewed Applications
Read 3 reviews rated 4 using NB100-57135 in the following applications:
Flow Cytometry Panel Builder
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Advanced Features
- Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
- Spillover Popups - Visualize the spectra of individual fluorochromes
- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
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Background: Histone H3
Histones are nuclear proteins responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Changes in chromatin structure play a large role in the regulation of transcription. The chromatin fibers are compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures.
Common histone modifications include methylation of lysine and arginine, acetylation of lysine, phosphorylation of threonine and serine, and sumoylation, biotinylation, and ubiquitylation of lysine. Posttranslational modifications such as acetylation of core histones regulates gene expression, thus altering protein function and regulation (1). Histone H3 is primarily acetylated at lysines 9, 14, 18, and 23 and have a theoretical molecular weight of 15 kDa. Acetylation at lysine 9 and 14 appears to control histone deposition, chromatin assembly and active transcription. Methylation of arginine residues within histone H3 has also been linked to transcription regulation. Histone H3 has been linked to various types of cancer as a biomarker through the aberrant expression of histone deacetylase (HDAC) enzymes and changes to chromatins (2-4).
References
1. Zhang, Y. X., Akumuo, R. C., Espana, R. A., Yan, C. X., Gao, W. J., & Li, Y. C. (2018). The histone demethylase KDM6B in the medial prefrontal cortex epigenetically regulates cocaine reward memory. Neuropharmacology, 141, 113-125. doi:10.1016/j.neuropharm.2018.08.030
2. Nandakumar, V., Hansen, N., Glenn, H. L., Han, J. H., Helland, S., Hernandez, K,...Meldrum, D. R. (2016). Vorinostat differentially alters 3D nuclear structure of cancer and non-cancerous esophageal cells. Sci Rep, 6, 30593. doi:10.1038/srep30593
3. Zhou, M., Li, Y., Lin, S., Chen, Y., Qian, Y., Zhao, Z., & Fan, H. (2019). H3K9me3, H3K36me3, and H4K20me3 Expression Correlates with Patient Outcome in Esophageal Squamous Cell Carcinoma as Epigenetic Markers. Dig Dis Sci, 64(8), 2147-2157. doi:10.1007/s10620-019-05529-2
4. Li, Y., Guo, D., Sun, R., Chen, P., Qian, Q., & Fan, H. (2019). Methylation Patterns of Lys9 and Lys27 on Histone H3 Correlate with Patient Outcome in Gastric Cancer. Dig Dis Sci, 64(2), 439-446. doi:10.1007/s10620-018-5341-8
Additional Histone H3 Products
Product Documents
Certificate of Analysis
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Product Specific Notices
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Related Research Areas
Citations for Histone H3 [Citrulline Arg17, Citrulline Arg2, Citrulline Arg8] Antibody
Customer Reviews (3)
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Customer Images
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Application: ImmunofluorescenceSample Tested: Brain tissueSpecies: MouseVerified Customer | Posted 03/11/2025Nucleus (Blue, DAPI) ; H3cit (green) Hemorrhagic stroke model FxFr ; 10 µm thickness 1:400 Secondary antibody AF488Nucleus (Blue, DAPI) ; H3cit (green) Hemorrhagic stroke model FxFr ; 10 µm thickness 1:400 Secondary antibody AF488
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Application: Western BlotSample Tested: mouse hepatocytes and HepG2 cellsSpecies: Human and MouseVerified Customer | Posted 11/25/2017
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Application: Western BlotSample Tested:Species: HumanVerified Customer | Posted 08/06/2016
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- 7-Amino Actinomycin D (7-AAD) Cell Viability Flow Cytometry Protocol
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ChIP Protocol Video
- Chromatin Immunoprecipitation (ChIP) Protocol
- Chromatin Immunoprecipitation Protocol
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
- Extracellular Membrane Flow Cytometry Protocol
- Flow Cytometry Protocol for Cell Surface Markers
- Flow Cytometry Protocol for Staining Membrane Associated Proteins
- Flow Cytometry Staining Protocols
- Flow Cytometry Troubleshooting Guide
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- How to Run an R&D Systems DuoSet ELISA
- How to Run an R&D Systems Quantikine ELISA
- How to Run an R&D Systems Quantikine™ QuicKit™ ELISA
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Intracellular Flow Cytometry Protocol Using Alcohol (Methanol)
- Intracellular Flow Cytometry Protocol Using Detergents
- Intracellular Nuclear Staining Flow Cytometry Protocol Using Detergents
- Intracellular Staining Flow Cytometry Protocol Using Alcohol Permeabilization
- Intracellular Staining Flow Cytometry Protocol Using Detergents to Permeabilize Cells
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Propidium Iodide Cell Viability Flow Cytometry Protocol
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Liperfluo
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Characterization of Human Th22 Cells
- Protocol for the Characterization of Human Th9 Cells
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- Quantikine HS ELISA Kit Assay Principle, Alkaline Phosphatase
- Quantikine HS ELISA Kit Principle, Streptavidin-HRP Polymer
- R&D Systems Quality Control Western Blot Protocol
- Sandwich ELISA (Colorimetric) – Biotin/Streptavidin Detection Protocol
- Sandwich ELISA (Colorimetric) – Direct Detection Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: ELISA
- Troubleshooting Guide: Fluorokine Flow Cytometry Kits
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars
FAQs
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Q: Can you provide NB100-57135 biotynilated?
A: Unfortunately, item NB100-57135 cannot be offered in a directly conjugated format as the base product is sold as unpurified antisera.
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Q: What is the source of histone material used for the western blot with NB100-57135?
A: NB100-57135 has been validated in western blot with HL60 cells treated with DMSO and calcimycin to induce citrullination.
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Q: Would you please advise us what samples you used to generate WB image with NB100-57135?
A: Our lab has just confirmed NB100-57135 has been validated in Western blot with HL60 cells treated with DMSO and calcimycin to induce citrullination.
-
Q: Can you provide NB100-57135 biotynilated?
A: Unfortunately, item NB100-57135 cannot be offered in a directly conjugated format as the base product is sold as unpurified antisera.
-
Q: What is the source of histone material used for the western blot with NB100-57135?
A: NB100-57135 has been validated in western blot with HL60 cells treated with DMSO and calcimycin to induce citrullination.
-
Q: Would you please advise us what samples you used to generate WB image with NB100-57135?
A: Our lab has just confirmed NB100-57135 has been validated in Western blot with HL60 cells treated with DMSO and calcimycin to induce citrullination.
-
Q: Can you provide NB100-57135 biotynilated?
A: Unfortunately, item NB100-57135 cannot be offered in a directly conjugated format as the base product is sold as unpurified antisera.
-
Q: What is the source of histone material used for the western blot with NB100-57135?
A: NB100-57135 has been validated in western blot with HL60 cells treated with DMSO and calcimycin to induce citrullination.
-
Q: Would you please advise us what samples you used to generate WB image with NB100-57135?
A: Our lab has just confirmed NB100-57135 has been validated in Western blot with HL60 cells treated with DMSO and calcimycin to induce citrullination.