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Figure 1. ChIP Chromatin Immunoprecipitation of H3R2me2sK4me2 antibody. Chromatin from one million formaldehyde cross-linked Hela cells was used with 2 μg of H3R2me2sK4me2 and 20 μl of magnetic IgG beads per immunoprecipitation. A no antibody (No Ab) control was also used. Immunoprecipitated DNA was quantified using quantitative PCR and normalized to the input chromatin.
Figure 2. Immunofluorescence Immunofluorescence of H3R2me2sK4me2 antibody. Tissue: HeLa cells. Fixation: 0.5% PFA. Primary antibody used at a 1:100 dilution for 1 h at RT. Secondary antibody: Dylight 488 secondary antibody at 1:10,000 for 45 min at RT. Localization: Histone H3R2me2sK4me2 is nuclear and chromosomal. Staining: Histone H3R2me2sK4me2 is expressed in green, nuclei and alpha-tubulin are counterstained with DAPI (blue) and Dylight 594 (red).
Figure 3. Western Blot Western Blot of H3R2me2sK4me2 antibody. 30 μg of C. elegans embryo cell lysate. Primary antibody used at a 1:500 dilution overnight at 4°C. Secondary antibody: IRDye800TM rabbit secondary antibody at 1:10,000 for 45 min at RT. Predicted/Observed size: ~15 kDa. Other band(s): None.
Figure 4. Western Blot Western Blot of H3R2me2sK4me2 antibody. 30 μg of NIH-3T3 histone extracts. Primary antibody used at 1:500 overnight at 4°C. Secondary antibody: IRDye800TM rabbit secondary antibody at 1:10,000 for 45 min at RT. Predicted/Observed size: ~15 kDa. Other band(s): None.
Figure 5. Dot Blot Dot Blot of H3R2me2sK4me2 antibody. Lane 1: R2me2. Lane 2: R2me2/K4me2. Lane 3: K4me2. Load: 0.1, 1, 0.5, 5, and 10 picomoles of peptide. Primary antibody used at a 1:1,000 dilution 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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Immunofluorescence using the Diagenode monoclonal antibody directed against CRISPR/Cas9
HeLa cells transfected with a Cas9 expression vector (... Read more
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