Histone H3.1 Antibodies
We offer Histone H3.1 Antibodies for use in common research applications: ELISA, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Paraffin, Western Blot. Each Histone H3.1 Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our Histone H3.1 Antibodies can be used in a variety of model species: Human, Mouse, Rat. Use the list below to choose the Histone H3.1 Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our Histone H3.1 polyclonal antibodies.
Alternate Names for Histone H3.1 Antibodies
anti-Histone H3.1 antibody, anti-HIST1H3E antibody, anti-H3 histone family, member D antibody, anti-H3.1HIST1H3D antibody, anti-H3/d antibody, anti-H3FA antibody, anti-H3FB antibody, anti-H3FC antibody, anti-H3FDHIST1H3F antibody, anti-H3FF antibody, anti-H3FH antibody, anti-H3FI antibody, anti-H3FJ antibody, anti-H3FK antibody, anti-H3FL antibody, anti-HIST1H3A antibody, anti-HIST1H3B antibody, anti-HIST1H3C antibody, anti-HIST1H3G antibody, anti-HIST1H3H antibody, anti-HIST1H3I antibody, anti-HIST1H3J antibody, anti-histone 1, H3e antibody, anti-histone cluster 1, H3e antibody, anti-Histone H3/a antibody, anti-Histone H3/b antibody, anti-Histone H3/c antibody, anti-Histone H3/d antibody, anti-Histone H3/f antibody, anti-Histone H3/h antibody, anti-Histone H3/i antibody, anti-Histone H3/j antibody, anti-Histone H3/k antibody, anti-Histone H3/l antibody
16 Results for "histone-h31" in Primary Antibodies
![Western Blot: Histone H3.1 Antibody [NBP2-75524] - Analysis of Histone H3.1 on F9 cell lysate using anti-Histone H3.1 antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/Histone-H3.1-Antibody-Western-Blot-NBP2-75524-img0005.jpg "Western Blot: Histone H3.1 Antibody [NBP2-75524] - Analysis of Histone H3.1 on F9 cell lysate using anti-Histone H3.1 antibody at 1/1,000 dilution.")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 Antibody [NBP2-75524] - Staining Histone H3.1 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/Histone-H3.1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-75524-img0003.jpg)
![Immunohistochemistry-Paraffin: Histone H3.1 Antibody [NBP2-75524] - Analysis of paraffin-embedded human liver tissue using anti-Histone H3.1 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/Histone-H3.1-Antibody-Immunohistochemistry-Paraffin-NBP2-75524-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 Antibody [NBP2-75524] - Staining Histone H3.1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/Histone-H3.1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-75524-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 Antibody [NBP2-75524] - Staining Histone H3.1 in PC-3M cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/Histone-H3.1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-75524-img0002.jpg)
![Immunohistochemistry: Histone H3.1 Antibody (27F2) [NBP3-26228] - Image of Histone H3.1 Antibody (27F2) diluted at 1:100 and staining in paraffin-embedded human glioma cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26228_rabbit-histone-h3-1-mab-27f2-2722024857331.jpg "Immunohistochemistry: Histone H3.1 Antibody (27F2) [NBP3-26228] - Image of Histone H3.1 Antibody (27F2) diluted at 1:100 and staining in paraffin-embedded human glioma cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.")
![Immunohistochemistry: Histone H3.1 Antibody (27F2) [NBP3-26228] - Image of Histone H3.1 Antibody (27F2) diluted at 1:100 and staining in paraffin-embedded human glioma cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26228_rabbit-histone-h3-1-mab-27f2-27220248471915.jpg)
![Western Blot: Histone H3.1 Antibody (27F2) [NBP3-26228] - Positive Western Blot detected in Jurkat whole cell lysate. All lanes: Histone H3.1 Antibody at 1.5ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26228_rabbit-histone-h3-1-mab-27f2-282202411485848.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 Antibody (27F2) [NBP3-26228] - Staining of Hela cells with Histone H3.1 Antibody (27F2) at 1:93, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26228_rabbit-histone-h3-1-mab-27f2-2822024132362.jpg)
![Flow Cytometry: Histone H3.1 Antibody (27F2) [NBP3-26228] - Overlay histogram showing Hela cells stained with Histone H3.1 Antibody (27F2) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min.The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4C. The secondary antibody used was FITC goat anti-rabbit IgG (H+L) at 1/200 dilution for 1 h at 4C. Control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26228_rabbit-histone-h3-1-mab-27f2-282202414183685.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 Antibody [NB100-81964] - Staining of methanol-fixed Hela cells using NB100-81964](http://images.novusbio.com/fullsize/antibody/Histone-H3.jpg "Immunocytochemistry/Immunofluorescence: Histone H3.1 Antibody [NB100-81964] - Staining of methanol-fixed Hela cells using NB100-81964")
![Western Blot: Histone H3. 1 Antibody [NB100-81964] - Western blot analysis of extracts of various cell lines, using NB100-81964](http://images.novusbio.com/fullsize/nb100-81964_rabbit-polyclonal-histone-h3-1-antibody-23420241452105.jpg)
![Western Blot: Histone H3.1 [Dimethyl Lys4] Antibody (6F6) [NBP3-26622] - Positive Western Blot detected in Mouse brain tissue, Mouse heart tissue. All lanes: Histone H3.1 [Dimethyl Lys4] Antibody at 0.55ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26622_rabbit-histone-h3-1-dimethyl-lys-4-mab-6f6-28220241136305.jpg "Western Blot: Histone H3.1 [Dimethyl Lys4] Antibody (6F6) [NBP3-26622] - Positive Western Blot detected in Mouse brain tissue, Mouse heart tissue. All lanes: Histone H3.1 [Dimethyl Lys4] Antibody at 0.55ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Dimethyl Lys4] Antibody (6F6) [NBP3-26622] - Analysis of Histone H3.1 [Dimethyl Lys4] Antibody (6F6) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26622_rabbit-histone-h3-1-dimethyl-lys-4-mab-6f6-2822024132365.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Dimethyl Lys4] Antibody (6F6) [NBP3-26622] - Staining of Hela cells with Histone H3.1 [Dimethyl Lys4] Antibody (6F6) at 1:34, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26622_rabbit-histone-h3-1-dimethyl-lys-4-mab-6f6-28220241312245.jpg)
![Flow Cytometry: Histone H3.1 [Dimethyl Lys4] Antibody (6F6) [NBP3-26622] - Overlay histogram showing Hela cells stained with Histone H3.1 [Dimethyl Lys4] Antibody (6F6) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min.The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4C. The secondary antibody used was FITC goat anti-rabbit IgG (H+L) at 1/200 dilution for 1 h at 4C. Control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26622_rabbit-histone-h3-1-dimethyl-lys-4-mab-6f6-282202414312754.jpg)
![Western Blot: Histone H3.1 [ac Lys14] Antibody (3H3) [NBP3-26533] - Positive Western Blot detected in Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate. Rat brain tissue. All lanes: Histone H3.1 [ac Lys14] Antibody at 0.75 ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26533_rabbit-histone-h3-1-ac-lys-14-mab-3h3-28220241152513.jpg "Western Blot: Histone H3.1 [ac Lys14] Antibody (3H3) [NBP3-26533] - Positive Western Blot detected in Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate. Rat brain tissue. All lanes: Histone H3.1 [ac Lys14] Antibody at 0.75 ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [ac Lys14] Antibody (3H3) [NBP3-26533] - Staining of Hela cells(treated by 15mM sodium butyrate for 30min) with Histone H3.1 [ac Lys14] Antibody (3H3) at 1:46, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26533_rabbit-histone-h3-1-ac-lys-14-mab-3h3-28220241249361.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [ac Lys14] Antibody (3H3) [NBP3-26533] - Analysis of Histone H3.1 [ac Lys14] Antibody (3H3) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26533_rabbit-histone-h3-1-ac-lys-14-mab-3h3-282202412493623.jpg)
![Western Blot: Histone H3.1 [Monomethyl Lys18] Antibody (2B5) [NBP3-26134] - Positive Western Blot detected in MCF-7 whole cell lysate. Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate, Rat brain tissue. All lanes: Histone H3.1 [Monomethyl Lys18] Antibody at 0.7ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26134_rabbit-histone-h3-1-monomethyl-lys-18-mab-2b5-28220241140934.jpg "Western Blot: Histone H3.1 [Monomethyl Lys18] Antibody (2B5) [NBP3-26134] - Positive Western Blot detected in MCF-7 whole cell lysate. Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate, Rat brain tissue. All lanes: Histone H3.1 [Monomethyl Lys18] Antibody at 0.7ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Lys18] Antibody (2B5) [NBP3-26134] - Analysis of Histone H3.1 [Monomethyl Lys18] Antibody (2B5) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26134_rabbit-histone-h3-1-monomethyl-lys-18-mab-2b5-2822024132360.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Lys18] Antibody (2B5) [NBP3-26134] - Staining of Hela cells with Histone H3.1 [Monomethyl Lys18] Antibody (2B5) at 1:43, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26134_rabbit-histone-h3-1-monomethyl-lys-18-mab-2b5-28220241312240.jpg)
![Western Blot: Histone H3.1 [Monomethyl Arg2] Antibody (4G5) [NBP3-26130] - Positive Western Blot detected in Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate. All lanes: Histone H3.1 [Monomethyl Arg2] Antibody at 0.95ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26130_rabbit-histone-h3-1-monomethyl-arg-2-mab-4g5-282202411363010.jpg "Western Blot: Histone H3.1 [Monomethyl Arg2] Antibody (4G5) [NBP3-26130] - Positive Western Blot detected in Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate. All lanes: Histone H3.1 [Monomethyl Arg2] Antibody at 0.95ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Arg2] Antibody (4G5) [NBP3-26130] - Staining of Hela cells with Histone H3.1 [Monomethyl Arg2] Antibody (4G5) at 1:60, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26130_rabbit-histone-h3-1-monomethyl-arg-2-mab-4g5-2822024132368.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Arg2] Antibody (4G5) [NBP3-26130] - Analysis of Histone H3.1 [Monomethyl Arg2] Antibody (4G5) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26130_rabbit-histone-h3-1-monomethyl-arg-2-mab-4g5-282202412493629.jpg)
![Western Blot: Histone H3.1 [ac Lys4] Antibody (4H6) [NBP3-26532] - Positive Western Blot detected in Hela whole cell lysate. treated by 15mM sodium butyrate for 30min. All lanes: Histone H3.1 [ac Lys4] Antibody at 1.1ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26532_rabbit-histone-h3-1-ac-lys-4-mab-4h6-28220241140935.jpg "Western Blot: Histone H3.1 [ac Lys4] Antibody (4H6) [NBP3-26532] - Positive Western Blot detected in Hela whole cell lysate. treated by 15mM sodium butyrate for 30min. All lanes: Histone H3.1 [ac Lys4] Antibody at 1.1ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [ac Lys4] Antibody (4H6) [NBP3-26532] - Staining of Hela cells(treated by 15mM sodium butyrate for 30min) with Histone H3.1 [ac Lys4] Antibody (4H6) at 1:68, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26532_rabbit-histone-h3-1-ac-lys-4-mab-4h6-282202412493616.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [ac Lys4] Antibody (4H6) [NBP3-26532] - Analysis of Histone H3.1 [ac Lys4] Antibody (4H6) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26532_rabbit-histone-h3-1-ac-lys-4-mab-4h6-282202412493648.jpg)
![Western Blot: Histone H3.1 [p Ser10] Antibody (2A5) [NBP3-26419] - Positive Western Blot detected in Hela whole cell lysate. MCF-7 whole cell lysate. PC3 whole cell lysate. All lanes: Histone H3.1 [p Ser10] Antibody at 0.5ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26419_rabbit-histone-h3-1-p-ser-10-mab-2a5-28220241152511.jpg "Western Blot: Histone H3.1 [p Ser10] Antibody (2A5) [NBP3-26419] - Positive Western Blot detected in Hela whole cell lysate. MCF-7 whole cell lysate. PC3 whole cell lysate. All lanes: Histone H3.1 [p Ser10] Antibody at 0.5ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [p Ser10] Antibody (2A5) [NBP3-26419] - Staining of Hela cells with Histone H3.1 [p Ser10] Antibody (2A5) at 1:31, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26419_rabbit-histone-h3-1-p-ser-10-mab-2a5-28220241323636.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [p Ser10] Antibody (2A5) [NBP3-26419] - Analysis of Histone H3.1 [p Ser10] Antibody (2A5) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26419_rabbit-histone-h3-1-p-ser-10-mab-2a5-282202412493625.jpg)
![Western Blot: Histone H3.1 [ac Lys56] Antibody (3H2) [NBP3-26534] - Positive Western Blot detected in: Hela whole cell lysate treated by 15mM sodium butyrate for 30min. All lanes: Histone H3.1 [ac Lys56] Antibody at 0.7ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution.Predicted band size: 15 KDaObserved band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26534_rabbit-histone-h3-1-ac-lys-56-mab-3h2-2822024114095.jpg "Western Blot: Histone H3.1 [ac Lys56] Antibody (3H2) [NBP3-26534] - Positive Western Blot detected in: Hela whole cell lysate treated by 15mM sodium butyrate for 30min. All lanes: Histone H3.1 [ac Lys56] Antibody at 0.7ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution.Predicted band size: 15 KDaObserved band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [ac Lys56] Antibody (3H2) [NBP3-26534] - Analysis of Histone H3.1 [ac Lys56] Antibody (3H2) diluted at 1:100 and staining in HepG2 cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26534_rabbit-histone-h3-1-ac-lys-56-mab-3h2-282202412475119.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [ac Lys56] Antibody (3H2) [NBP3-26534] - Staining of Hela cells(treated by 15mM sodium butyrate for 30min) with Histone H3.1 [ac Lys56] Antibody (3H2) at 1:43, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26534_rabbit-histone-h3-1-ac-lys-56-mab-3h2-28220241323621.jpg)
![Western Blot: Histone H3.1 [Monomethyl Lys36] Antibody (1F4) [NBP3-26133] - Positive Western Blot detected in HepG2 whole cell lysate. SH-SY5Y whole cell lysate. Rat brain tissue. All lanes: Histone H3.1 [Monomethyl Lys36] Antibody at 0.6ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26133_rabbit-histone-h3-1-monomethyl-lys-36-mab-1f4-28220241148583.jpg "Western Blot: Histone H3.1 [Monomethyl Lys36] Antibody (1F4) [NBP3-26133] - Positive Western Blot detected in HepG2 whole cell lysate. SH-SY5Y whole cell lysate. Rat brain tissue. All lanes: Histone H3.1 [Monomethyl Lys36] Antibody at 0.6ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Lys36] Antibody (1F4) [NBP3-26133] - Staining of Hela cells with Histone H3.1 [Monomethyl Lys36] Antibody (1F4) at 1:37.5, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26133_rabbit-histone-h3-1-monomethyl-lys-36-mab-1f4-282202412475136.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Lys36] Antibody (1F4) [NBP3-26133] - Analysis of Histone H3.1 [Monomethyl Lys36] Antibody (1F4) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26133_rabbit-histone-h3-1-monomethyl-lys-36-mab-1f4-282202412493646.jpg)
![Western Blot: Histone H3.1 [Monomethyl Arg17] Antibody (3E10) [NBP3-26131] - Positive Western Blot detected in Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate. All lanes: Histone H3.1 [Monomethyl Arg17] Antibody at 1.55ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26131_rabbit-histone-h3-1-monomethyl-arg-17-mab-3e10-282202411472138.jpg "Western Blot: Histone H3.1 [Monomethyl Arg17] Antibody (3E10) [NBP3-26131] - Positive Western Blot detected in Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate. All lanes: Histone H3.1 [Monomethyl Arg17] Antibody at 1.55ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Arg17] Antibody (3E10) [NBP3-26131] - Staining of Hela cells withHistone H3.1 [Monomethyl Arg17] Antibody (3E10) at 1:96, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26131_rabbit-histone-h3-1-monomethyl-arg-17-mab-3e10-28220241312210.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Arg17] Antibody (3E10) [NBP3-26131] - Analysis of Histone H3.1 [Monomethyl Arg17] Antibody (3E10) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26131_rabbit-histone-h3-1-monomethyl-arg-17-mab-3e10-282202412475141.jpg)