HSC-T6 cells were subjected to SDS PAGE followed by western blot with 84446-2-RR (Acetyl-Histone H2B (Lys16) antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.
HSC-T6 cells were subjected to SDS PAGE followed by western blot with 84446-2-RR (Acetyl-Histone H2B (Lys16) antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.
WB analysis of NIH/3T3 using 84446-2-RR
NIH/3T3 cells were subjected to SDS PAGE followed by western blot with 84446-2-RR (Acetyl-Histone H2B (Lys16) antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.
NIH/3T3 cells were subjected to SDS PAGE followed by western blot with 84446-2-RR (Acetyl-Histone H2B (Lys16) antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.
IF Staining of NIH/3T3 using 84446-2-RR
Immunofluorescent analysis of (4% PFA) fixed Trichostatin A treated NIH/3T3 cells using Acetyl-Histone H2B (Lys16) antibody (84446-2-RR, Clone: 241194C7 ) at dilution of 1:1000 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).
Immunofluorescent analysis of (4% PFA) fixed Trichostatin A treated C6 cells using Acetyl-Histone H2B (Lys16) antibody (84446-2-RR, Clone: 241194C7 ) at dilution of 1:1000 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).
IF Staining of HeLa using 84446-2-RR
Immunofluorescent analysis of (4% PFA) fixed HeLa cells using Acetyl-Histone H2B (Lys16) antibody (84446-2-RR, Clone: 241194C7 ) at dilution of 1:200 and Multi-rAb CoraLite ® Plus 488-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (RGAR002).
Immunofluorescent analysis of (4% PFA) fixed HeLa cells using Acetyl-Histone H2B (Lys16) antibody (84446-2-RR, Clone: 241194C7 ) at dilution of 1:200 and Multi-rAb CoraLite ® Plus 488-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (RGAR002).
Dot Blot experiment of peptide using 84446-2-RR
Dot blot analysis was used to confirm the specificity of Acetyl-Histone H2B (Lys16) antibody. Acetylated peptides were spotted onto NC and probed with antibody at 1 µg/ml.The amount of peptide (μg/mL) spotted is indicated next to each row.
Dot blot analysis was used to confirm the specificity of Acetyl-Histone H2B (Lys16) antibody. Acetylated peptides were spotted onto NC and probed with antibody at 1 µg/ml.The amount of peptide (μg/mL) spotted is indicated next to each row.
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HSC-T6 cells were subjected to SDS PAGE followed by western blot with 84446-2-RR (Acetyl-Histone H2B (Lys16) antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.
WB analysis of NIH/3T3 using 84446-2-RR
NIH/3T3 cells were subjected to SDS PAGE followed by western blot with 84446-2-RR (Acetyl-Histone H2B (Lys16) antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.
IF/ICC Figures
IF Staining of NIH/3T3 using 84446-2-RR
Immunofluorescent analysis of (4% PFA) fixed Trichostatin A treated NIH/3T3 cells using Acetyl-Histone H2B (Lys16) antibody (84446-2-RR, Clone: 241194C7 ) at dilution of 1:1000 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).
IF Staining of C6 using 84446-2-RR
Immunofluorescent analysis of (4% PFA) fixed Trichostatin A treated C6 cells using Acetyl-Histone H2B (Lys16) antibody (84446-2-RR, Clone: 241194C7 ) at dilution of 1:1000 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).
IF Staining of HeLa using 84446-2-RR
Immunofluorescent analysis of (4% PFA) fixed HeLa cells using Acetyl-Histone H2B (Lys16) antibody (84446-2-RR, Clone: 241194C7 ) at dilution of 1:200 and Multi-rAb CoraLite ® Plus 488-Goat Anti-Rabbit Recombinant Secondary Antibody (H+L) (RGAR002).
DOT BLOT Figures
Dot Blot experiment of peptide using 84446-2-RR
Dot blot analysis was used to confirm the specificity of Acetyl-Histone H2B (Lys16) antibody. Acetylated peptides were spotted onto NC and probed with antibody at 1 µg/ml.The amount of peptide (μg/mL) spotted is indicated next to each row.
The species listed in Tested Reactivity are in-house verified and applicable species. For unlisted species, please refer to the homology analysis of the immunogen sequence and related species. For rabbit polyclonal antibodies, homology >70% is recommended. For mouse monoclonal antibodies and rabbit recombinant antibodies, homology >90% is recommended. Generally, the higher the homology, the greater the applicability. However, there will be certain differences in protein expression in different species, tissues or cells. Therefore, the homology analysis results are for reference only and do not serve as a guarantee.
