- Home
- Companies
- Agrisera AB - part of Olink® Group
- Products
- Agrisera - Model E(z) - Histone-Lysine ...
Agrisera - Model E(z) -Histone-Lysine N-Methyltransferase
Histone-lysine N-methyltransferase (Ez) is a Polycomb group (PcG) protein, and a catalytic subunit of the Esc/E(z) complex. By methylating Lys-9 and Lys-27 of histone H3, this complex is involved in transcriptional repression of target genes. E(z) is important for the repression during the first six hours of embryogenesis. The Esc/E(z) complex, together with the recruitment of the PRC1 complex, is necessary for the repression of homeotic target genes. Alternative names: Lysine N-methyltransferase 6, Protein enhancer of zeste.
- AS16 3935 - Clonality: Polyclonal - Host: Rabbit - Reactivity: Drosophila melanogaster
- Immunogen: GST-fusion with amino acids 8-190 of the Drosophila melanogaster E(z) protein, UniProt: P42124
- Host: Rabbit
- Clonality: Polyclonal
- Purity: Affinity purified and depleted of anti-GST antibodies, in PBS pH 7.4
- Format: Lyophilized
- Quantity: 50 µg
- Reconstitution: For reconstitution add 50 µl, of sterile water.
- Storage: Lyophilized antibody can be stored at -20°C for up to 3 years. Re-constituted antibody can be stored at 4°C for several days to weeks.
- Once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.
- Tested applications: Chromatin Immunoprecipitation (ChIP).
- Recommended dilution: 3 µg/IP (ChIP)
- Expected | apparent MW: 86.9 kDa
- Confirmed reactivity: Drosophila melanogaster
- Predicted reactivity: Bactrocera cucurbitae, Bactrocera dorsalis, Bactrocera latifrons, Ceratitis capitata, Lucilia cuprina
- Selected references: To be added when available, antibody released in June 2016
ChIP and qPCR analysis were done as described [Schwartz YB, Kahn TG, Nix DA, Li XY, Bourgon R, et al. (2006) Genome-wide analysis of Polycomb targets in Drosophila melanogaster. Nat Genet 38: 700–705. doi: 10.1038/ng1817]. Chromatin from Su(z)12 mutant cell line (Kahn T. et all, submitted) served as a negative control, chromatin from Ras3 cells served as a positive control. Quantitative PCR was performed with primers specific for BXD-PRE of Ubx gene (Polycomb target gene in repressed state), used as positive controls, and for intergenic region, used as negative control. Figure 1 shows the ChIP recovery, measured by qPCR as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA). Chromatin from 5x107 cells and 3mg of anti-E(z) antibody were used for each ChIP reaction.
Courtesy of Dr. Tatyana Khan, Umeå University, Sweden.