H2Bpan polyclonal antibody

Catalog Number
50 μg/18 μl
  Bulk order

Polyclonal antibody raised in rabbit against histone H2B using a KLH-conjugated synthetic peptide containing an unmodified sequence from the C-terminal part of the protein.

Concentration2.8 µg/µl
Species reactivityHuman
PurityPeptide affinity purified
Storage ConditionsStore at -20°C; for long storage, store at -80°C. Avoid multiple freeze-thaw cycles.
Storage BufferPBS containing 0.05% azide.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Applications Suggested dilution References
ChIP * 0.5 - 1 µg/IP Fig 1
ELISA 1:1,000 - 1/5,000 Fig 2
WB 1:2,000 - 1/10,000 Fig 3
IF 1:1,000 Fig 3

* Please note that the optimal antibody amount per IP should be determined by the end-user. We recommend testing 1-5 µg per IP.

  • Validation Data


    Figure 1 ChIP results obtained with the Diagenode antibody directed against H2B
    ChIP assays were performed using human HeLa cells, the Diagenode antibody against H2B (cat. No. C15410157) and optimized PCR primer sets for qPCR. ChIP was performed with the Auto Histone ChIP-seq” kit (Cat. No. C01010022) on sheared chromatin from 1 million cells using the IP-Star automated system. A titration of the antibody consisting of 0.5, 1, 2 and 5 µg per ChIP experiment was analysed. IgG (2 µg/IP) was used as negative IP control. QPCR was performed with primers for the promoters of the active GAPDH and EIF4A2 genes, used as negative controls and for the inactive MYOD1 gene and the Sat2 satellite repeat, used as positive 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 Determination of the titer
    To determine the titer of the antibody, an ELISA was performed using a serial dilution of the Diagenode antibody directed against H2B (C15410157) in antigen coated wells. By plotting the absorbance against the antibody dilution (Figure 2), the titer of the antibody was estimated to be 1:40,000.

    Western Blot

    Figure 3 Western blot analysis using the Diagenode antibody directed against H2B
    Western blot was performed on whole cell extracts from HeLa cells (40 µg, lane 1) and on 1 µg of recombinant histone H2B (lane 2) using the Diagenode antibody against H2B (Cat. No. C15410157). The antibody was diluted 1:10,000 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.


    Immunofluorescence using the Diagenode antibody directed against H2B
    HeLa cells were stained with the Diagenode antibody against H2B (Cat. No. C15410157) and with DAPI. Cells were fixed with 4% formaldehyde for 10’ and blocked with PBS/TX-100 containing 1% BSA. The cells were immunofluorescently labeled with the H2B antibody (middle) diluted 1:1,000 in blocking solution followed by an anti-rabbit antibody conjugated to Alexa488. The left panel shows staining of the nuclei with DAPI. A merge of the two stainings is shown on the right.

  •  Applications
    Enzyme-linked immunosorbent assay. Read more
    ChIP-qPCR (ab)
    Read more
    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. Learn more about: Load... Read more
  •  Documents
    Datasheet H2Bpan pAb-157-050 DATASHEET
    Datasheet description
  •  Publications

    How to properly cite this product in your work

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