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Figure 1. ChIP Chromatin Immunoprecipitation with the H4S1p antibody. Chromatin from one million formaldehyde cross-linked HeLa cells was used with 2 ug of H4S1p alongside a no antibody (No Ab) control. DNA was measured by qPCR and normalized to total input.
Figure 2. Immunofluorescence Immunofluorescence with the H4S1p antibody. Tissue: Nonmitotic, prophase, and telophase HeLa cells. Fixation: 0.5% PFA. Primary antibody used at a 1:50 dilution for 1 h at RT. Secondary antibody: FITC secondary antibody at 1:10,000 for 45 min at RT. Localization: Histone H4S1p is nuclear. Staining: Histone H4S1p is expressed in green, nuclei and alpha-tubulin are counterstained with DAPI (blue) and Dylight 594 (red).
Figure 3. Immunofluorescence Immunofluorescence with the H4S1p antibody. Tissue: Nonmitotic and telophase HeLa cells. Fixation: 0.5% PFA. Primary antibody used at a 1:50 dilution for 1 h at RT. Secondary antibody: FITC secondary antibody at 1:10,000 for 45 min at RT. Localization: Histone H4S1p is nuclear. Staining: Histone H4S1p is expressed in green, nuclei and alpha-tubulin are counterstained with DAPI (blue) and Dylight 594 (red).
Figure 4. Western Blot Western Blot with the H4S1p antibody. 30 μg HeLa histone extracts. Primary antibody used at 1:1000 dilution overnight at 4°C. Secondary antibody: IRDye800TM rabbit secondary antibody at a 1:10,000 for 45 min at RT. Predicted/Observed size: ~13 kDa. Other band(s): None.
Figure 5. Dot Blot Dot Blot with the H4S1p antibody. Lane 1: H4S1 unmodfied. Lane 2: H4S1p. Lane 3: H4S1 unmodified. Load: 1, 10, and 100 picomoles of peptide. Primary antibodyused at 0,1 μg/ml for 45 min at 4°C. Secondary antibody: DylightTM488 rabbit secondary antibody at 1:10,000 for 45 min at RT.
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