H4K5,8,12,16ac Antibody

Figure 1. ChIP results obtained with the antibody directed against H4K5,8,12,16ac
ChIP assays were performed using human HeLa cells, the antibody against H4K5,8,12,16ac (cat. No. C15410024) and optimized PCR primer sets for qPCR. ChIP was performed with the iDeal ChIP-seq kit (cat. No. C01010051) 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 promoter of the active gene EIF4A2 and for a region 1 kb upstream of the GAPDH gene, used as positive controls, and for the inactive MYOD1 gene and the Sat2 satellite repeat region 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. ChIP-seq results obtained with the antibody directed against H4K5,8,12,16ac
ChIP was performed with 2 µg of the antibody against H4K5,8,12,16ac (cat. No. C15410024) on sheared chromatin from 1 million HeLa cells using the iDeal ChIP-seq kit as described above. The IP’d DNA was subsequently analysed on an Illumina Genome Analyzer. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 36 bp tags were aligned to the human genome using the ELAND algorithm. Figure 2 shows the signal distribution along the complete length of chromosome 5 (figure 2A) and a zoomin to a 600 kb region (figure 2B). Figure 2C and D show the enrichment in two genomic regions on chromosome 3 and 12, respectively, containing the EIF4A2 and GAPDH positive controls. The position of the amplicon used for validating the QPCR results is shown with an arrow.

Figure 3. CUT&Tag results obtained with the antibody directed against H4K5,8,12,16ac
CUT&Tag was performed on 50,000 K562 cells using 1 µg of the antibody against H4K5,8,12,16ac (cat. No. C15410024) and the Universal CUT&Tag kit (cat. No. C01070024). The libraries were subsequently analysed on an Illumina NovaSeqX sequencer (2x150 bp paired-end reads) according to the manufacturer’s instructions. The tags were aligned to the human genome (hg38) using the BWA algorithm. Figure 2 shows the peak distribution along the complete sequence and a 600 kb region of the X-chromosome (figure 3A and B) and in 2 genomic regions on chromosome 7 and 12 (figure 3C and D, respectively).

Figure 4. Determination of the antibody titer
To determine the titer of the antibody, an ELISA was performed using a serial dilution of the antibody directed against H4K5,8,12,16ac (cat. No. C15410024) in antigen coated wells. The antigen used was a peptide containing the histone modification of interest. By plotting the absorbance against the antibody dilution (Figure 4), the titer of the antibody was estimated to be 1:21,200

Figure 5. Cross reactivity tests using the antibody directed against H4K5,8,12,16ac
To test the cross reactivity of the antibody against H4K5,8,12,16ac (cat. No. C15410024), a Dot Blot analysis was performed with peptides containing other histone modifications and the unmodified H4. One hundred to 0.2 pmol of the respective peptides were spotted on a membrane. The antibody was used at a dilution of 1:20,000. Figure 5 shows a high specificity of the antibody for the modification of interest.

Figure 6. Immunofluorescence using the antibody directed against H4K5,8,12,16ac
Mouse NIH3T3 cells were stained with the antibody against H4K5,8,12,16ac (cat. No. C15410024) and with DAPI. Cells were fixed with 4% formaldehyde for 10’ and blocked with PBS/TX-100 containing 5% normal goat serum and 1% BSA. The cells were immunofluorescently labelled with the H4K5,8,12,16ac antibody (left) diluted 1:500 in blocking solution followed by an anti-rabbit antibody conjugated to Alexa488. The middle panel shows staining of the nuclei with DAPI. A merge of the two stains is shown on the right.