Various lysates were subjected to SDS PAGE followed by western blot with 86768-1-RR (Acetyl-Histone H4 (Lys91) antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours.
Various lysates were subjected to SDS PAGE followed by western blot with 86768-1-RR (Acetyl-Histone H4 (Lys91) antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours.
WB analysis of HSC-T6 using 86768-1-RR
Trichostatin A treated HSC-T6 cells were subjected to SDS PAGE followed by western blot with 86768-1-RR (Acetyl-Histone H4 (Lys91) antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours.
Trichostatin A treated HSC-T6 cells were subjected to SDS PAGE followed by western blot with 86768-1-RR (Acetyl-Histone H4 (Lys91) antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours.
IF Staining of HeLa using 86768-1-RR
Immunofluorescent analysis of (4% PFA) fixed Trichostatin A treated HeLa cells using Acetyl-Histone H4 (Lys91) antibody (86768-1-RR, Clone: 251157D9 ) at dilution of 1:2000 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).
Immunofluorescent analysis of (4% PFA) fixed Trichostatin A treated HeLa cells using Acetyl-Histone H4 (Lys91) antibody (86768-1-RR, Clone: 251157D9 ) at dilution of 1:2000 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).
Dot Blot experiment of / using 86768-1-RR
Dot blot analysis was used to confirm the specificity of 86768-1-RR Acetyl-Histone H4 (Lys91) antibody. 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 86768-1-RR Acetyl-Histone H4 (Lys91) antibody. 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.
ChIP experiment of HeLa using 86768-1-RR
Chromatin was prepared from HeLa cells. Cells were fixed with formaldehyde for 10 minutes. The ChIP was performed with 15 µg of cross-linked chromatin, 5 µg of Acetyl-Histone H4 (Lys91) (86768-1-RR) or 5 ug of Normal Rabbit IgG (98136-1-RR), and 20 µl of Protein A Magarose Beads. The immunoprecipitated DNA was quantified by real-time PCR.
Chromatin was prepared from HeLa cells. Cells were fixed with formaldehyde for 10 minutes. The ChIP was performed with 15 µg of cross-linked chromatin, 5 µg of Acetyl-Histone H4 (Lys91) (86768-1-RR) or 5 ug of Normal Rabbit IgG (98136-1-RR), and 20 µl of Protein A Magarose Beads. The immunoprecipitated DNA was quantified by real-time PCR.
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Various lysates were subjected to SDS PAGE followed by western blot with 86768-1-RR (Acetyl-Histone H4 (Lys91) antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours.
WB analysis of HSC-T6 using 86768-1-RR
Trichostatin A treated HSC-T6 cells were subjected to SDS PAGE followed by western blot with 86768-1-RR (Acetyl-Histone H4 (Lys91) antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours.
IF/ICC Figures
IF Staining of HeLa using 86768-1-RR
Immunofluorescent analysis of (4% PFA) fixed Trichostatin A treated HeLa cells using Acetyl-Histone H4 (Lys91) antibody (86768-1-RR, Clone: 251157D9 ) at dilution of 1:2000 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), CL594-Phalloidin (red).
DOT BLOT Figures
Dot Blot experiment of / using 86768-1-RR
Dot blot analysis was used to confirm the specificity of 86768-1-RR Acetyl-Histone H4 (Lys91) antibody. 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.
CHIP-QPCR Figures
ChIP experiment of HeLa using 86768-1-RR
Chromatin was prepared from HeLa cells. Cells were fixed with formaldehyde for 10 minutes. The ChIP was performed with 15 µg of cross-linked chromatin, 5 µg of Acetyl-Histone H4 (Lys91) (86768-1-RR) or 5 ug of Normal Rabbit IgG (98136-1-RR), and 20 µl of Protein A Magarose Beads. The immunoprecipitated DNA was quantified by real-time PCR.
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.
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