Anti-Histone H3 (methyl K37) antibody [EPR20970]

7 product images

• 

  Western blot - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728)

  Blocking/Dilution buffer: 5% NFDM/TBST.
  

  The recombinant proteins were His-tagged.

  All lanes: Western blot - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728) at 1/1000 dilution

  Lane 1: Unmodified recombinant H3 10 ng

  Lane 2: Recombinant mutant H3 chemically modified to mimic H3K37Me, 10ng

  Lane 3: Recombinant mutant H3 chemically modified to mimic H3K37Me2 10 ng

  Lane 4: Recombinant mutant H3 chemically modified to mimic H3K37Me3 10 ng

  Secondary

  All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

  Predicted band size: 15 kDa

  Exposure time: 3min

• 

  Immunocytochemistry/ Immunofluorescence - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728)

  Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized NIH/3T3 (mouse embryonic fibroblast cell line) cells labeling Histone H3 (methyl K37) with ab215728 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 AlexaFluor^®488 Goat anti-Rabbit secondary antibody at 1/1000 dilution (green). Confocal image showing nuclear staining in NIH/3T3 cell line is observed. DAPI was used as the nuclear counterstain. Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor^® 594)(Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889) was used as the counterstain antibody at 1/200 dilution (red).
  

  Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 AlexaFluor^®488 Goat anti-Rabbit secondary at 1/1000 dilution.

• 

  Flow Cytometry (Intracellular) - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728)

  Intracellular flow cytometric analysis of 90% methanol permeabilized , 4% paraformaldehyde-fixed NIH/3T3 (mouse embryo fibroblast cell line) cells labeling Histone H3 (methyl K37) with ab215728 at 1/60 dilution (Red) compared withRabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat anti rabbit IgG (Alexa Fluor^® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 was used as the secondary antibody.
  

• 

  Western blot - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728)

  Exposure times:
  Lane 1: 26 seconds;
  Lane 2: 3 minutes;
  Lane 3: 81 seconds;
  Lane 4: 3 minutes.
  

  Blocking/Dilution buffer: 5% BSA/TBST

  All lanes: Western blot - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728) at 1/1000 dilution

  Lane 1: NCCIT (human pluripotent embryonic carcinoma epithelial cell) whole cell lysate at 10 µg

  Lane 2: HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 10 µg

  Lane 3: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 10 µg

  Lane 4: PC-12 (rat adrenal gland pheochromocytoma) whole cell lysate at 10 µg

  Secondary

  All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

  Predicted band size: 15 kDa

• 

  Immunocytochemistry/ Immunofluorescence - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728)

  Immunofluorescent analysis of 4% paraformaldehyde-fixed 0.1% Triton X-100 permeabilized HeLa (human cervix adenocarcinoma epithelial cell line) cells labeling Histone H3 (methyl K37) with ab215728 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 AlexaFluor^®488 Goat anti-Rabbit secondary antibody at 1/1000 dilution (green). Confocal image showing nuclear staining in HeLa cell line is observed. DAPI was used as the nuclear counterstain. Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor^® 594)(Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889) was used as the counterstain antibody at 1/200 dilution (red).
  

  Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 AlexaFluor^®488 Goat anti-Rabbit secondary at 1/1000 dilution.

• 

  Flow Cytometry (Intracellular) - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728)

  Intracellular flow cytometric analysis of 90% methanol permeabilized , 4% paraformaldehyde-fixed HeLa (human cervix adenocarcinoma epithelial cell) cells labeling Histone H3 (methyl K37) with ab215728 at 1/60 dilution (Red) compared withRabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat anti rabbit IgG (Alexa Fluor^® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 was used as the secondary antibody.
  

• 

  Peptide Array - Anti-Histone H3 (methyl K37) antibody [EPR20970] (ab215728)

  ab215728 was tested in Peptide Array against 501 different modified and unmodified histone peptides; each peptide is printed on the array at six concentrations (each in triplicate).

  Blocking buffer: 5% BSA in TBST.

  Primary antibody concentration: 0.1 µg/ml.

  Circle area represents affinity between the antibody and a peptide: all antigen-containing peptides are displayed as red circles, all other peptides as blue circles. The affinity is calculated as area under curve when antibody binding values are plotted against the corresponding peptide concentration. Each circle area is normalized to the peptide with the strongest affinity.

  The complete dataset, including full list of all peptides and information on the position of each peptide in the diagram, is available under the Support & downloads section.