Anti-Ku70 antibody [EPR4027] - BSA and Azide free

7 product images

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  Immunoprecipitation - Anti-Ku70 antibody [EPR4027] - BSA and Azide free (ab239912)

  Anti-Ku70 antibody [EPR4027] ab92450 (purified ) at 1/20 dilution (0.5ug) immunoprecipitating Ku70 in HeLa whole cell lysate.
  

  Lane 1 (input): HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate 10μg.
  Lane 2 (+): Anti-Ku70 antibody [EPR4027] ab92450 & HeLa whole cell lysate.
  Lane 3 (-): Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Ku70 antibody [EPR4027] ab92450 in HeLa whole cell lysate.

  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-Ku70 antibody [EPR4027] ab92450).

  All lanes: Immunoprecipitation - Anti-Ku70 antibody [EPR4027] (Anti-Ku70 antibody [EPR4027] ab92450)

  Predicted band size: 70 kDa

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  Flow Cytometry (Intracellular) - Anti-Ku70 antibody [EPR4027] - BSA and Azide free (ab239912)

  Intracellular Flow Cytometry analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling Ku70 with purified Anti-Ku70 antibody [EPR4027] ab92450 at 1/20 dilution (5μg/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-Ku70 antibody [EPR4027] ab92450).

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  Immunocytochemistry/ Immunofluorescence - Anti-Ku70 antibody [EPR4027] - BSA and Azide free (ab239912)

  Immunocytochemistry/ Immunofluorescence analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling Ku70 with purified Anti-Ku70 antibody [EPR4027] ab92450 at 1/250 dilution (0.46 μg/ml). Cells were fixed in 100% Methanol and permeabilized with None. 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) 1/200 (2.5 μg/ml). 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-Ku70 antibody [EPR4027] ab92450).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ku70 antibody [EPR4027] - BSA and Azide free (ab239912)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human colon carcinoma tissue sections labeling Ku70 with purified Anti-Ku70 antibody [EPR4027] ab92450 at 1/250 dilution (0.46 μg/ml). Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 1 (pH 6.0). Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101) 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-Ku70 antibody [EPR4027] ab92450).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ku70 antibody [EPR4027] - BSA and Azide free (ab239912)

  Paraffin embedded Human testis tissue (A) or Human tonsil tissue (B) were labelled with Anti-Ku70 antibody [EPR4027] ab92450 at 1/100 dilution.
  

  Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Ku70 antibody [EPR4027] ab92450).

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  Immunocytochemistry/ Immunofluorescence - Anti-Ku70 antibody [EPR4027] - BSA and Azide free (ab239912)

  Immunofluorescence staining of HeLa cells using Anti-Ku70 antibody [EPR4027] ab92450 at 1/100 dilution.This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Ku70 antibody [EPR4027] ab92450).

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  Flow Cytometry (Intracellular) - Anti-Ku70 antibody [EPR4027] - BSA and Azide free (ab239912)

  Overlay histogram showing HeLa cells stained with Anti-Ku70 antibody [EPR4027] ab92450 (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-Ku70 antibody [EPR4027] ab92450, 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. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa 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-Ku70 antibody [EPR4027] ab92450).