WB
Western blot analysis of various lysates using SMARCA2 / BRM Rabbit mAb at 1:1000 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: 10 s.
ICC/IF
Immunofluorescence analysis of HeLa cellsusing SMARCA2 / BRM Rabbit mAb at dilution of 1:100 (40x lens). Secondaryantibody: Cy3-conjugated Goat anti-RabbitIgG (H+L) at 1:500 dilution. Blue:DAPI for nuclear staining.
IHC
Immunohistochemistry analysis of paraffinembedded Human cervix cancer tissue usingSMARCA2 / BRM Rabbit mAb atdilution of 1:200 (40x lens). High pressureantigen retrieval performed with 0.01MCitrate Buffer (pH 6.0) prior to IHC staining.
IP
Immunoprecipitation analysis of 300 μg extracts of Hela cells using 3 μg SMARCA2 / BRM Rabbit mAb. Western blot was performed from the immunoprecipitate using SMARCA2 / BRM Rabbit mAb at a dilition of 1:5000.
ChIP
Chromatin immunoprecipitation was performed with 20 μg of cross-linked chromatin from MCF7 cellstreated with β-estradiol (10 nM, 45 min), using 5 μg of SMARCA2 / BRM Rabbit mAb and RabbitIgG isotype control. The enrichment of immunoprecipitated DNA at different genomic loci wasexamined by quantitative PCR. The histogram compares the ratio of the immunoprecipitated DNA to theinput at given loci.