Anti-MUC1 antibody [EPR1023] - BSA and Azide free

10 product images

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Immunohistochemical staining of paraffin embedded human endometrium with purified Anti-MUC1 antibody [EPR1023] ab109185 at a working dilution of 1 in 500. The secondary antibody used is a HRP polymer for rabbit IgG. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC1 antibody [EPR1023] ab109185).

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  Immunoprecipitation - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Anti-MUC1 antibody [EPR1023] ab109185 (purified) at 1/20 immunoprecipitating MUC1 in T47-D (Lane 1). Lane 2 - PBS. For western blotting, a HRP-conjugated anti-rabbit IgG, specific to the non-reduced form of IgG was used as the secondary antibody (1/1500).

  Blocking buffer and concentration: 5% NFDM/TBST.

  Diluting buffer and concentration: 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-MUC1 antibody [EPR1023] ab109185).

  All lanes: Immunoprecipitation - Anti-MUC1 antibody [EPR1023] (Anti-MUC1 antibody [EPR1023] ab109185)

  Predicted band size: 122 kDa

  Observed band size: 18-25 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Immunohistochemical staining of paraffin embedded mouse lung with purified Anti-MUC1 antibody [EPR1023] ab109185 at a working dilution of 1 in 500. The secondary antibody used is a HRP polymer for rabbit IgG. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC1 antibody [EPR1023] ab109185).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Immunohistochemical staining of paraffin embedded rat kidney with purified Anti-MUC1 antibody [EPR1023] ab109185 at a working dilution of 1 in 500. The secondary antibody used is a HRP polymer for rabbit IgG. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC1 antibody [EPR1023] ab109185).

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  Immunocytochemistry/ Immunofluorescence - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Immunofluorescence staining of A431 cells with purified Anti-MUC1 antibody [EPR1023] ab109185 at a working dilution of 1 in 1000, counter-stained with DAPI. The secondary antibody was Alexa Fluor^® 555 goat anti rabbit, used at a dilution of 1 in 400. 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, purified Anti-MUC1 antibody [EPR1023] ab109185 was used at a dilution of 1/200 followed by an Alexa Fluor^® 555 goat anti-mouse antibody at a dilution of 1/500.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC1 antibody [EPR1023] ab109185).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Anti-MUC1 antibody [EPR1023] ab109185 (unpurified) showing positive staining in Breast ductal infiltrating carcinoma tissue.
  

  Perform heat mediated antigen retrieval 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-MUC1 antibody [EPR1023] ab109185).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Anti-MUC1 antibody [EPR1023] ab109185 (unpurified) showing positive staining in Normal stomach tissue.
  
  

  Perform heat mediated antigen retrieval 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-MUC1 antibody [EPR1023] ab109185).

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  Flow Cytometry (Intracellular) - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Overlay histogram showing MCF7 cells fixed in 2% PFA and stained with purified Anti-MUC1 antibody [EPR1023] ab109185 at a dilution of 1 in 30 (pink line). The secondary antibody used was FITC goat anti-rabbit at a dilution of 1 in 150. Rabbit monoclonal IgG was used as an isotype control.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC1 antibody [EPR1023] ab109185).

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  Flow Cytometry (Intracellular) - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  Overlay histogram showing MCF7 cells stained with unpurified Anti-MUC1 antibody [EPR1023] ab109185 (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 (Anti-MUC1 antibody [EPR1023] ab109185, 1/1000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor^® 488 goat anti-rabbit IgG (H&L) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1μg/1x10⁶ cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. 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 MCF7 cells fixed with 4% paraformaldehyde (10 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-MUC1 antibody [EPR1023] ab109185).

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  OI-RD Scanning - Anti-MUC1 antibody [EPR1023] - BSA and Azide free (ab271879)

  We have systematically measured KD (the equilibrium dissociation constant between the antibody and its antigen), of more than 840 recombinant antibodies to assess not only their individual KD values but also to see the average affinity of antibody.
  Based on the comparison with published literature values for mouse monoclonal antibodies, Recombinant antibodies appear to be on average 1-2 order of magnitude higher affinity.