Anti-NQO1 antibody [A180]

10 product images

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  This image is courtesy of an anonymous customer review

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NQO1 antibody [A180] (ab28947)

  Immunohistochemical analysis of dog skin tissue, staining NQO1 with ab28947.
  
  Tissue was fixed with formaldehyde and antigen retrieval was by heat mediation in a citrate buffer (pH 6). Samples were incubated with primary antibody (1/175 in BSA in TBS) for 45 minutes. Rabbit Anti-Mouse IgG H&L (Biotin) preadsorbed ab98784 rabbit polyclonal to anti-mouse HRP (IgG) (1/500) was used as the secondary antibody.

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  Flow Cytometry (Intracellular) - Anti-NQO1 antibody [A180] (ab28947)

  Overlay histogram showing HeLa cells stained with ab28947 (red line). The cells were fixed with 80% methanol (5 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 (ab28947, 1μg/1x10⁶ cells) for 30 min at 22°C. The secondary antibody used was goat anti-mouse DyLight® 488 (IgG H+L) (Goat Anti-Mouse IgG H&L (DyLight® 488) preadsorbed ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (Mouse IgG1, Kappa Monoclonal [B11/6] - Isotype Control ab91353/ab>, 2μg/1x10⁶ cells) used under the same conditions. Acquisition of >5,000 events was performed.
  
  

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  Immunocytochemistry/ Immunofluorescence - Anti-NQO1 antibody [A180] (ab28947)

  ab28947 staining NQO1 in HepG2 cells. The cells were fixed with 100% methanol (5 min), permeabilized with 0.1% PBS-Tween for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1%PBS-Tween for 1h. The cells were then incubated overnight at 4°C with ab28947 at 5µg/ml and Anti-beta Tubulin antibody - Loading Control ab6046, Rabbit polyclonal to beta Tubulin - Loading Control. Cells were then incubated with Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed ab150117, Goat polyclonal Secondary Antibody to Mouse IgG H&L (Alexa Fluor^® 488) preadsorbed at 1/1000 dilution (shown in green) and Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080, Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor^® 594) at 1/1000 dilution (shown in pseudocolour red). Nuclear DNA was labelled with DAPI (shown in blue).

  Image was acquired with a high-content analyser (Operetta CLS, Perkin Elmer) and a maximum intensity projection of confocal sections is shown.

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  Western blot - Anti-NQO1 antibody [A180] (ab28947)

  Lane 1: Marker

  Lane 2: Western blot - Anti-NQO1 antibody [A180] (ab28947) at 1 µg/mL

  All lanes: Kidney (Human) Tissue Lysate (ab7920) at 20 µg

  Secondary

  All lanes: IRDye 680 Conjugated Goat Anti-Mouse IgG (H+L) at 1/10000 dilution

  Predicted band size: 31 kDa

  Observed band size: 30 kDa

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  Western blot - Anti-NQO1 antibody [A180] (ab28947)

  Lane 1: Wild-type HAP1 whole cell lysate (20 μg)
  Lane 2: NQO1 knockout HAP1 whole cell lysate (20 μg)
  Lane 3: HepG2 whole cell lysate (20 μg)
  

  Lanes 1 - 3: Merged signal (red and green). Green - ab28947 observed at 31 kDa. Red - loading control, Anti-alpha Tubulin antibody [EPR13478(B)] - Loading Control ab176560, observed at 50 kDa.

  ab28947 was shown to specifically react with NQO1 in wild-type HAP1 cells as signal was lost in NQO1 knockout cells. Wild-type and NQO1 knockout samples were subjected to SDS-PAGE. ab28947 and Anti-alpha Tubulin antibody [EPR13478(B)] - Loading Control ab176560 (Rabbit anti-alpha Tubulin loading control) were incubated overnight at 4°C at 1 μg/ml and 1/20000 dilution respectively. Blots were developed with Goat anti-Mouse IgG H&L (IRDye^® 800CW) preabsorbed Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772 and Goat anti-Rabbit IgG H&L (IRDye^® 680RD) preabsorbed Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.

  All lanes: Western blot - Anti-NQO1 antibody [A180] (ab28947)

  Predicted band size: 31 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NQO1 antibody [A180] (ab28947)

  IHC image of NQO1 staining in sections of formalin fixed paraffin embedded normal human pancreas* (left) and human pancreas adenocarcinoma* (right), performed on a Leica BOND^TM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab28947, 0.1μg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
  

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NQO1 antibody [A180] (ab28947)

  IHC image of NQO1 staining in human breast adenocarcinoma formalin fixed paraffin embedded tissue section, performed on a Leica Bond system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab28947, 0.1μg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Sandwich ELISA - Anti-NQO1 antibody [A180] (ab28947)

  Sandwich ELISA for the detection of NQO1, using ab28947 (1/500) as the capture antibody and Anti-NQO1 antibody ab34173 (1/1000) for the detection.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NQO1 antibody [A180] (ab28947)

  Human breast cancer tissue stained with ab28947 NQO1 antibody.

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  This image is courtesy of an anonymous customer review

  Sandwich ELISA - Anti-NQO1 antibody [A180] (ab28947)

  Sandwich ELISA for the detection of NQO1. ab28947 (1/500) was used as the capture antibody. A rabbit polyclonal raised againts the C-terminal end of NQO1 was used for the detection. Please refer to abreview for further experimental details.