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Applications: ChIP (1 - 2 µl/ChIP)
ELISA (1:3000)
WB (1:1000)
IF (1:500)
Assay Conditions: ChIP results obtained with the monoclonal antibody directed against H3K27me3
ChIP assays were performed using human HeLa cells, the monoclonal antibody against H3K27me3 (Cat. No. 25243) and optimized PCR primer sets for qPCR. ChIP was performed on sheared chromatin from 1 million cells. A titration of the antibody consisting of 1, 2, 5, and 10 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 genes c-fos and GAPDH as negative controls, and for the coding regions of the inactive genes MYT1 and TSH2B 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). These results are in accordance with the observation that H3K27me3 is preferably present at inactive genes.Cross reactivity of the monoclonal antibody directed against H3K27me3
To test the specificity an ELISA was performed using a serial dilution of the monoclonal antibody against H3K27me3 (Cat. No. 25243). The wells were coated with peptides containing the unmodified H3K27 region as well as the mono-, di- and trimethylated H3K27 and the trimethylated H3K9. Figure 2 shows a high specificity of the antibody for the peptide containing the modification of interest.Western blot analysis using the monoclonal antibody directed against H3K27me3
Histone extracts (15 µg) from HeLa cells were analysed by Western blot using the monoclonal antibody against H3K27me3 (Cat. No. 25243) 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.Immunofluorescence using the monoclonal antibody directed against H3K27me3
HeLa cells were stained with the antibody against H3K27me3 (Cat. No. 25243) and with DAPI. Cells were fixed with 4% formaldehyde for 10 minutes and blocked with PBS/TX-100 containing 5% normal goat serum and 1% BSA. The cells were immunofluorescently labelled with the H3K27me3 antibody (left) diluted 1:500 in blocking solution followed by an anti-mouse antibody conjugated to Alexa594. The middle panel shows staining of the nuclei with DAPI. A merge of the two stainings is shown on the right.
Background: Trimethylation of lysine 27 on H3 has been strongly related to transcriptional repression in numerous important processes during development and diseases of both plants and animals. This modification is maintained by the Polycomb Repressive Complex 2 (catalyzed by EZH2 methyltransferase) and can be removed by lysine demethylases such as JMJD3.
Concentration: 50 µg/50 µl
Description: Monoclonal antibody raised in mouse against histone H3 trimethylated at lysine 27 (H3K27me3), using a KLH-conjugated synthetic peptide
Format: Aqueous buffer solution
Formulation: PBS containing 0.05% azide and 0.05% ProClin 300
Immunogen: synthetic peptide
Purification: Protein A purified
Storage Stability: Store at -80°C for up to 2 years. Centrifuge after first thaw to maximize product recovery. Aliquot to avoid repeated freeze/thaw cycles. Aliquots may be stored at -20°C for at least one month.
Uniprot: P68431
Warnings: Avoid freeze/thaw cycles.
Biosafety Level: Not applicable (BSL-1)
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