Anti-Histone H2A antibody - ChIP Grade
| Name | Anti-Histone H2A antibody - ChIP Grade |
|---|---|
| Supplier | Abcam |
| Catalog | ab15653 |
| Prices | $385.00 |
| Sizes | 100 µg |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Applications | WB IHC-P ICC/IF ICC/IF ChIP |
| Species Reactivities | Human, Mouse |
| Antigen | Synthetic peptide corresponding to Human Histone H2A aa 100 to the C-terminus (C terminal) conjugated to Keyhole Limpet Haemocyanin (KLH) |
| Blocking Peptide | Human Histone H2A peptide |
| Description | Rabbit Polyclonal |
| Gene | HIST1H2AE |
| Conjugate | Unconjugated |
| Supplier Page | Shop |
Product images
All lanes : Anti-Histone H2A antibody - ChIP Grade (ab15653) at 0.5 µg/mlLane 1 : HeLa nuclear extractLane 2 : HeLa nuclear extract with Human Histone H2A peptide (ab15660) at 1 µg/ml
Chromatin was prepared from Hela cells according to the Abcam X-ChIP protocol. Cells were fixed with formaldehyde for 10min. The ChIP was performed with 25µg of chromatin, 2µg of ab15653 (blue), and 20µl of Protein A/G sepharose beads. No antibody was added to the beads control (yellow). The immunoprecipitated DNA was quantified by real time PCR (Taqman approach). Primers and probes are located in the first kb of the transcribed region.
Image courtesy of Human Protein Atlas ab15653 staining histone H2A in human male kidney, showing a distinct and strong nuclear staining pattern in tubuli and glomeruli. Paraffin embedded human skin tissue was incubated with ab15653 (1/5000 dilution) for 30 mins at room temperature. Antigen retrieval was performed by heat induction in citrate buffer pH 6. ab15653 was tested in a tissue microarray (TMA) containing a wide range of normal and cancer tissues as well as a cell microarray consisting of a range of commonly used, well characterised human cell lines. Further results for this antibody can be found at www.proteinatlas.org.
ICC/IF image of ab15653 stained human HeLa cells. The cells were 4% PFA fixed (10 min), permabilised in 0.1% PBS-Tween (20 min) and incubated with the antibody (ab15653, 1µg/ml) for 1h at room temperature. 1%BSA / 10% normal goat serum / 0.3M glycine was used to block non-specific protein-protein interactions. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red). DAPI was used to stain the cell nuclei (blue).
Product References
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Reitsma JM, Sato H, Nevels M, Terhune SS, Paulus C. J Virol. 2013 Oct;87(19):10763-76.
Analysis of chromatin dynamics during glucocorticoid receptor activation. - Analysis of chromatin dynamics during glucocorticoid receptor activation.
Burd CJ, Ward JM, Crusselle-Davis VJ, Kissling GE, Phadke D, Shah RR, Archer TK. Mol Cell Biol. 2012 May;32(10):1805-17.