Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free

9 product images

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  Multiplex immunohistochemistry - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  This data was developed using the same antibody clone in a different buffer formulation (Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827).
  

  Multiplex immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of rat pancreas tissue.

  Panel A: Merged staining of anti-Pancreatic Polypeptide (Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827, green), anti-Somatostatin 28 (Anti-Somatostatin 28 antibody [EPR3359(2)] ab111912, red) and DAPI (blue).

  Panel B: Anti-Pancreatic Polypeptide (green) stained on PP cells in rat pancreas islet.

  Panel C: Anti-Somatostatin 28 (red) stained on delta cells in rat pancreas islet.

  Panel D: Nuclear counter stain, DAPI (blue).

  Key protocol steps: The section was incubated in two rounds of staining with Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 (1/20000 dilution) and Anti-Somatostatin 28 antibody [EPR3359(2)] ab111912 (1/2000 dilution) for 30 mins at room temperature. Each round was followed by tyramide signal amplification with the appropriate fluorophore. Heat mediated antigen retrieval was used (Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins after every round of antibody/fluorophore staining.

  The immunostaining was performed on a Leica Biosystems BOND® RX instrument.

  A ready-to-use anti-Rabbit and Mouse Polymer HRP was used as a secondary.

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  Immunohistochemical analysis of paraffin-embedded rat pancreas tissue labeling Pancreatic Polypeptide with Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 at 1/5000 dilution, followed by Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining on PP cells in rat pancreas islet (PMID: 27270601) is observed. Counter stained with hematoxylin.
  Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).
  

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.

  The section was incubated with Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 for 10 mins at RT.

  The immunostaining was performed on a Leica Biosystems BOND^® RX instrument.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827).

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  Immunohistochemical analysis of paraffin-embedded mouse pancreas tissue labeling Pancreatic Polypeptide with Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 at 1/5000 dilution, followed by Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining on PP cells in mouse pancreas islet (PMID: 27270601) is observed. Counter stained with hematoxylin.
  Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).
  

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.

  The section was incubated with Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 for 10 mins at RT.

  The immunostaining was performed on a Leica Biosystems BOND^® RX instrument.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827).

• 

  Immunohistochemistry (Frozen sections) - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  Immunohistochemical analysis of frozen section of 4%PFA-fixed, 0.2% Triton X-100 permeabilized rat pancreas tissue labeling Pancreatic Polypeptide with Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody at 1/1000 dilution (green). Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 and Anti-Insulin antibody [K36aC10] ab6995 are shown to stain PP cells and beta cells of rat pancreatic islets respectively (PMID: 24825414). The nuclear counter stain is DAPI (blue). Insulin is detected using Anti-Insulin antibody [K36aC10] ab6995, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor^® 594) preadsorbed (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at 1/1000 dilution (red).
  

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

  Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827).

• 

  Immunohistochemistry (Frozen sections) - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  Immunohistochemical analysis of frozen section of 4%PFA-fixed, 0.2% Triton X-100 permeabilized mouse pancreas tissue labeling Pancreatic Polypeptide with Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 488) (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody at 1/1000 dilution (green). Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 and Anti-Insulin antibody [K36aC10] ab6995 are shown to stain PP cells and beta cells of mouse pancreatic islet respectively (PMID: 24825414). The nuclear counter stain is DAPI (blue). Insulin is detected using Anti-Insulin antibody [K36aC10] ab6995, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor^® 594) preadsorbed (Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120) at 1/1000 dilution (red).
  

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

  Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827).

• 

  Multiplex immunohistochemistry - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  Fluorescence multiplex immunohistochemical analysis of the rat pancreas (Formalin/PFA-fixed paraffin-embedded sections).

  Panel A: merged staining of anti-SV2A (yellow; Opal™520), anti-GIP (magenta; Opal™570) and anti-Pancreatic Polypeptide (green; Opal™690) on rat pancreas.
  
  Panel B: anti-SV2A staining predominantly the beta cells in mouse pancreas islet.
  
  Panel C: anti-GIP staining the alpha cells in rat pancreas islet.
  
  Panel D: anti-Pancreatic Polypeptide staining the PP cells in rat pancreas islet.

  Nuclear DNA was labelled with DAPI (shown in blue). The section was incubated in three rounds of staining: in the order of Anti-SV2A antibody [EPR23500-32] ab254351 at 1/1000 dilution (0.48 μg/ml), Anti-GIP antibody [EPR20410] - BSA and Azide free ab271989 at 1/4000 dilution (0.25 μg/ml) and Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 at 1/10000 dilution (0.05 μg/ml) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  This data was developed using Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827, the same antibody clone in a different buffer formulation.

• 

  Multiplex immunohistochemistry - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  Fluorescence multiplex immunohistochemical analysis of the mouse pancreas (Formalin/PFA-fixed paraffin-embedded sections).

  Panel A: merged staining of anti-SV2A (yellow; Opal™520), anti-GIP (magenta; Opal™570) and anti-Pancreatic Polypeptide (green; Opal™690) on mouse pancreas.
  
  Panel B: anti-SV2A staining predominantly the beta cells in mouse pancreas islet.
  
  Panel C: anti-GIP staining the alpha cells in mouse pancreas islet.
  
  Panel D: anti-Pancreatic Polypeptide staining the PP cells in mouse pancreas islet.

  Nuclear DNA was labelled with DAPI (shown in blue). The section was incubated in three rounds of staining: in the order of Anti-SV2A antibody [EPR23500-32] ab254351 at 1/1000 dilution (0.48 μg/ml), Anti-GIP antibody [EPR20410] - BSA and Azide free ab271989 at 1/4000 dilution (0.25 μg/ml) and Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 at 1/10000 dilution (0.05 μg/ml) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  This data was developed using Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827, the same antibody clone in a different buffer formulation.

• 

  Multiplex immunohistochemistry - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  Fluorescence multiplex immunohistochemical analysis of the mouse pancreas (Formalin/PFA-fixed paraffin-embedded sections).

  Panel A: merged staining of anti-Somatostatin 28 (yellow; Opal™520), anti-GIP (magenta; Opal™570) and anti-Pancreatic Polypeptide (green; Opal™690) on mouse pancreas.
  
  Panel B: anti-Somatostatin 28 staining the delta cells in mouse pancreas islet.
  
  Panel C: anti-GIP staining the alpha cells in mouse pancreas islet.
  
  Panel D: anti-Pancreatic Polypeptide staining the PP cells in mouse pancreas islet.

  Nuclear DNA was labelled with DAPI (shown in blue). The section was incubated in three rounds of staining: in the order of Anti-Somatostatin 28 antibody [EPR3359(2)] ab111912 at 1/9000 dilution (0.07 μg/ml), Anti-GIP antibody [EPR20410] - BSA and Azide free ab271989 at 1/4000 dilution (0.25 μg/ml) and Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 at 1/10000 dilution (0.05 μg/ml) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  This data was developed using Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 , the same antibody clone in a different buffer formulation.

• 

  Multiplex immunohistochemistry - Anti-Pancreatic Polypeptide antibody [EPR22853-61] - BSA and Azide free (ab256592)

  Fluorescence multiplex immunohistochemical analysis of the rat pancreas (Formalin/PFA-fixed paraffin-embedded sections).

  Panel A: merged staining of anti-Somatostatin 28 (yellow; Opal™520), anti-GIP (magenta; Opal™570) and anti-Pancreatic Polypeptide (green; Opal™690) on rat pancreas.
  
  Panel B: anti-Somatostatin 28 staining the delta cells in rat pancreas islet.
  
  Panel C: anti-GIP staining the alpha cells in rat pancreas islet.
  
  Panel D: anti-Pancreatic Polypeptide staining the PP cells in rat pancreas islet.

  Nuclear DNA was labelled with DAPI (shown in blue). The section was incubated in three rounds of staining: in the order of Anti-Somatostatin 28 antibody [EPR3359(2)] ab111912 at 1/9000 dilution (0.07 μg/ml), Anti-GIP antibody [EPR20410] - BSA and Azide free ab271989 at 1/4000 dilution (0.25 μg/ml) and Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827 at 1/10000 dilution (0.05 μg/ml) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  This data was developed using Anti-Pancreatic Polypeptide antibody [EPR22853-61] ab255827, the same antibody clone in a different buffer formulation.