WB
Western blot analysis of various lysates using Histone H3 Rabbit mAb at 1:160000 dilutionincubated overnight at 4℃.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 20 s.
WB
Western blot analysis of lysates from HeLa cells using Histone H3 Rabbit mAb at1:10000-1:1280000 dilution incubated overnight at 4℃.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L)at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 20 s.
IHC
Immunohistochemistry analysis of paraffinembedded Mouse brain tissue using HistoneH3 Rabbit mAb at a dilution of1:5500 (40x lens). High pressure antigenretrieval performed with 0.01M Tris-EDTABuffer (pH 9.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffinembedded Human colon tissue using HistoneH3 Rabbit mAb at a dilution of1:5500 (40x lens). High pressure antigenretrieval performed with 0.01M Tris-EDTABuffer (pH 9.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffinembedded Rat lung tissue using Histone H3Rabbit mAb at a dilution of 1:5500(40x lens). High pressure antigen retrievalperformed with 0.01M Tris-EDTA Buffer (pH9.0) prior to IHC staining.
IP
Immunoprecipitation of Histone H3 from 200 µg extracts of MCF7 cells was performed using 2 µg ofHistone H3 Rabbit mAb. Rabbit Control IgG was used to precipitate the Control IgGsample. IP samples were eluted with 1× Laemmli Buffer. The Input lane represents 10% of the total input.Western blot analysis of immunoprecipitates was conducted using Histone H3 Rabbit mAb at adilution of 1:5000.
ChIP
Chromatin immunoprecipitation was performed with 10 μg of cross-linked chromatin from HeLa, using 2μg of Histone H3 Rabbit mAb and Rabbit IgG isotype control. The enrichment ofimmunoprecipitated DNA at different genomic loci was examined by quantitative PCR. The histogramcompares the ratio of the immunoprecipitated DNA to the input at given loci.