WB
Western blot analysis of various lysates using MonoMethyl-Histone H3-K4 Rabbit mAb at 1:5000dilution 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: 90 s.
WB
Western blot analysis of various lysates using MonoMethyl-Histone H3-K4 Rabbit mAb at1:10000 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: 45 s.
ICC/IF
Confocal imaging of HeLa cells usingMonoMethyl-Histone H3-K4 Rabbit mAb(dilution 1:200) followed by afurther incubation with Cy3-conjugated GoatAnti-Rabbit IgG (H+L) (dilution 1:500) (Red). The cells were counterstained with αTubulin Mouse mAb (dilution 1:400)followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L)(dilution 1:500) (Green). DAPI wasused for nuclear staining (Blue). Objective:100x.
ICC/IF
Confocal imaging of NIH/3T3 cells usingMonoMethyl-Histone H3-K4 Rabbit mAb( dilution 1:200) followed by afurther incubation with Cy3-conjugated GoatAnti-Rabbit IgG (H+L) (dilution 1:500) (Red). The cells were counterstained with αTubulin Mouse mAb (dilution 1:400)followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L)(dilution 1:500) (Green). DAPI wasused for nuclear staining (Blue). Objective:100x.
ICC/IF
Confocal imaging of C6 cells usingMonoMethyl-Histone H3-K4 Rabbit mAb(dilution 1:200) followed by afurther incubation with Cy3-conjugated GoatAnti-Rabbit IgG (H+L) (dilution 1:500)(Red). The cells were counterstained with αTubulin Mouse mAb (dilution 1:400)followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L)(dilution 1:500) (Green). DAPI wasused for nuclear staining (Blue). Objective:100x.
IHC
Immunohistochemistry analysis of paraffinembedded Mouse brain tissue usingMonoMethyl-Histone H3-K4 Rabbit mAb at a dilution of 1:16000 (40x lens).High pressure antigen retrieval performedwith 0.01M Tris-EDTA Buffer (pH 9.0) prior toIHC staining.
IHC
Immunohistochemistry analysis of paraffinembedded Human colon tissue usingMonoMethyl-Histone H3-K4 Rabbit mAb at a dilution of 1:16000 (40x lens).High pressure antigen retrieval performedwith 0.01M Tris-EDTA Buffer (pH 9.0) prior toIHC staining.
IHC
Immunohistochemistry analysis of paraffinembedded Rat brain tissue usingMonoMethyl-Histone H3-K4 Rabbit mAb at a dilution of 1:16000 (40x lens).High pressure antigen retrieval performedwith 0.01M Tris-EDTA Buffer (pH 9.0) prior toIHC staining.
ChIP
Chromatin immunoprecipitation was performed with 10 μg of cross-linked chromatin from HeLa, using 0.5μg of MonoMethyl-Histone H3-K4 Rabbit mAb and Rabbit IgG isotype control. Theenrichment of immunoprecipitated DNA at different genomic loci was examined by quantitative PCR. Thehistogram compares the ratio of the immunoprecipitated DNA to the input at given loci.
DB
Dot-blot analysis of all sorts of peptidesusing MonoMethyl-Histone H3-K4 Rabbit mAb at 1:1000 dilution.