WB
Western blot analysis of various lysates using MonoMethyl-Histone H3-K4 Rabbit pAb at 1:5000 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.
Negative control (NC): H3 protein.
Exposure time: 90 s.
DB
Dot-blot analysis of all sorts of peptides using MonoMethyl-Histone H3-K4 Rabbit pAb at 1:1000 dilution.
IHC
Immunohistochemistry analysis of paraffin-embedded Mouse kidney tissue using MonoMethyl-Histone H3-K4 Rabbit pAb at a dilution of 1:4000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffin-embedded Mouse lung tissue using MonoMethyl-Histone H3-K4 Rabbit pAb at a dilution of 1:4000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffin-embedded Rat colon tissue using MonoMethyl-Histone H3-K4 Rabbit pAb at a dilution of 1:4000 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IHC staining.
ICC/IF
Confocal imaging of HeLa cells using MonoMethyl-Histone H3-K4 Rabbit pAb followed by a further incubation with Cy3-conjugated Goat anti-Rabbit IgG (H+L) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.
CHIP
Chromatin immunoprecipitation was performed with 10 μg of cross-linked chromatin from HeLa cells, using 3 μg of MonoMethyl-Histone H3-K4 Rabbit pAb and Rabbit IgG isotype control. The enrichment of immunoprecipitated DNA at different genomic loci was examined by quantitative PCR. The histogram compares the ratio of the immunoprecipitated DNA to the input at given loci.