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Figure 1. ChIP results obtained with the Diagenode antibody directed against H3R2me2(asym) ChIP assays were performed using HeLa cells, the Diagenode antibody against H3R2me2(asym) (Cat. No. C15410316) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the inactive HBB and NANOG promoters, used as positive controls, and for the active EIF4A2 and GAPDH promoters, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
Figure 2. Western blot analysis using the Diagenode antibody directed against H3R2me2(asym) Histone extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against H3R2me2(asym) (Cat. No. C15410316). The antibody was diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.
WB Western blot : The quality of antibodies used in this technique is crucial for correct and specific protein identification. Diagenode offers huge selection of highly sensitive and specific western blot-validated antibodies.
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