Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free

10 product images

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Rat liver tissue sections labeling RanGAP1 with purified Anti-RanGAP1 antibody [EPR3295] ab92360 at 1/500 dilution (0.22 μg/ml). Perform heat mediated antigen retrieval using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0). ImmunoHistoProbe one step HRP Polymer (ready to use) was used as the secondary antibody. Negative control: PBS instead of the primary antibody. Hematoxylin was used as a counterstain.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

• 

  Immunocytochemistry/ Immunofluorescence - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Immunocytochemistry/ Immunofluorescence analysis of MCF7 (Human breast adenocarcinoma epithelial cell) cells labeling RanGAP1 with purified Anti-RanGAP1 antibody [EPR3295] ab92360 at 1/100 dilution (1.1 μg/ml). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor^® 594) at 1/200 (2.5 μg/ml) dilution. Goat anti rabbit IgG (Alexa Fluor^® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) was used as the secondary antibody at 1/1000 (2 μg/ml) dilution. DAPI (blue) was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

• 

  Immunoprecipitation - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Anti-RanGAP1 antibody [EPR3295] ab92360 (purified) at 1/20 dilution (0.5ug) immunoprecipitating RanGAP1 in HeLa whole cell lysates.
  Lane 1: HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates 10ug
  Lane 2 (+): Anti-RanGAP1 antibody [EPR3295] ab92360 & HeLa whole cell lysates
  Lane 3 (-): Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-RanGAP1 antibody [EPR3295] ab92360 in HeLa whole cell lysates
  For western blotting, VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/1000 dilution.
  Blocking and diluting buffer: 5% NFDM/TBST.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

  All lanes: Immunoprecipitation - Anti-RanGAP1 antibody [EPR3295] (Anti-RanGAP1 antibody [EPR3295] ab92360)

  Predicted band size: 63 kDa

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Mouse testis tissue sections labeling RanGAP1 with purified Anti-RanGAP1 antibody [EPR3295] ab92360 at 1/500 dilution (0.22 μg/ml). Perform heat mediated antigen retrieval using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0). ImmunoHistoProbe one step HRP Polymer (ready to use) was used as the secondary antibody. Negative control: PBS instead of the primary antibody. Hematoxylin was used as a counterstain.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

• 

  Immunocytochemistry/ Immunofluorescence - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Immunofluorescence staining of MCF7 cells with purified Anti-RanGAP1 antibody [EPR3295] ab92360 at a working dilution of 1/500, counter-stained with DAPI. The secondary antibody was an Alexa Fluor^® 488 conjugated goat anti-rabbit (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077), used at a dilution of 1/1000. The cells were fixed in 4% PFA and permeabilized using 0.1% Triton X 100. The negative control is shown in bottom right hand panel - for the negative control, PBS was used instead of the primary antibody.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human bladder carcinoma tissue sections labeling RanGAP1 with purified Anti-RanGAP1 antibody [EPR3295] ab92360 at 1/500 dilution (0.22 μg/ml). Perform heat mediated antigen retrieval using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0). ImmunoHistoProbe one step HRP Polymer (ready to use) was used as the secondary antibody. Negative control: PBS instead of the primary antibody. Hematoxylin was used as a counterstain.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

• 

  This image is courtesy of an anonymous customer review.

  Immunocytochemistry/ Immunofluorescence - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Anti-RanGAP1 antibody [EPR3295] ab92360 staining RanGAP1 in mouse hepatocyte cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with paraformaldehyde, permeabilized, and blocked with 2% BSA for 2 hours at 22°C. Samples were incubated with primary antibody (1/100 in blocking buffer) for 18 hours at 4°C. An Alexa Fluor® 488-conjugated goat anti-rabbit IgG polyclonal (1/10000) was used as the secondary antibody.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  b92360 at 1/100 dilution staining RanGAP1 in paraffin-embedded (1) Human breast carcinoma tissue and (2) Human testis tissue by immunohistochemistry.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

  Perform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.

• 

  Flow Cytometry (Intracellular) - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Overlay histogram showing Jurkat cells stained with Anti-RanGAP1 antibody [EPR3295] ab92360 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (Anti-RanGAP1 antibody [EPR3295] ab92360, 1/100 dilution) for 30 min at 22°C. The secondary antibody used was DyLight^® 488 goat anti-rabbit IgG (H+L) (Goat Anti-Rabbit IgG H&L (DyLight® 488) preadsorbed ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1μg/1x10⁶ cells) used under the same conditions. Unlabelled sample (blue line). Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in Jurkat cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).

• 

  Flow Cytometry (Intracellular) - Anti-RanGAP1 antibody [EPR3295] - BSA and Azide free (ab239907)

  Intracellular Flow Cytometry analysis of Jurkat (Human T cell leukemia T lymphocyte) cells labeling RanGAP1 with purified Anti-RanGAP1 antibody [EPR3295] ab92360 at 1/20 dilution (10μg/ml) (red). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor^® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody was used at 1/2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-RanGAP1 antibody [EPR3295] ab92360).