Anti-Histone H4 (butyryl K12) antibody
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(2 Publications )
Rabbit Polyclonal Histone H4 butyryl K12 antibody. Suitable for ICC, IP, ChIP, WB, ICC/IF and reacts with Human samples. Cited in 2 publications. Immunogen corresponding to Synthetic Peptide within Human H4C1 buK12.
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H4/A, H4FA, HIST1H4A, H4C2, H4/I, H4FI, HIST1H4B, H4C3, H4/G, H4FG, HIST1H4C, H4C4, H4/B, H4FB, HIST1H4D, H4C5, H4/J, H4FJ, HIST1H4E, H4C6, H4/C, H4FC, HIST1H4F, H4C8, H4/H, H4FH, HIST1H4H, H4C9, H4/M, H4FM, HIST1H4I, H4C11, H4/E, H4FE, HIST1H4J, H4C12, H4/D, H4FD, HIST1H4K, H4C13, H4/K, H4FK, HIST1H4L, H4C14, H4/N, H4F2, H4FN, HIST2H4, HIST2H4A, H4C15, H4/O, H4FO, HIST2H4B, H4C16, H4-16, HIST4H4, H4C1, Histone H4, H4K12bu
- ICC
Supplier Data
Immunocytochemistry - Anti-Histone H4 (butyryl K12) antibody (AB241120)
HeLa (human epithelial cell line from cervix adenocarcinoma) cells (treated with 30 mM sodium butyrate for 4 hours) labeling Histone H4 (butyryl K12) with ab241120 at 1/150 dilution in ICC.
The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Histone H4 (butyryl K12) antibody (AB241120)
HeLa (human epithelial cell line from cervix adenocarcinoma) cells (treated with 30 mM sodium butyrate for 4 hours) labeling Histone H4 (butyryl K12) with ab241120 at 1/75 dilution in ICC/IF.
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 4°C. The secondary antibody was Alexa Fluor®488-conjugated Goat anti-Rabbit IgG (H+L).
- ChIP
Supplier Data
ChIP - Anti-Histone H4 (butyryl K12) antibody (AB241120)
HeLa (human epithelial cell line from cervix adenocarcinoma); (106, treated with 30mM sodium butyrate for 4 hours) were treated with micrococcal nuclease, sonicated, and immunoprecipitated with 5 μg ab241120 or a control normal rabbit IgG. The resulting ChIP DNA was quantified using real-time PCR with primers against the β-Globin promoter.
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Publications (2)
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Nature metabolism 7:196-211 PubMed39789354
2025
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Nature communications 15:996 PubMed38307858
2024
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