Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free

15 product images

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  Immunohistochemistry (Frozen sections) - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat colon tissue labeling MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 AlexaFluor^® 488 Goat anti-Rabbit secondary at 1/1000 (2 μg/ml) dilution (Green). Positive staining on rat colon is observed. The nuclear counterstain was DAPI (Blue).
  

  Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 AlexaFluor^® 488 Goat anti-Rabbit secondary at 1/1000 (2 μg/ml) 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-MUC2 antibody [EPR23479-47] ab272692).

• 

  Immunohistochemistry (Frozen sections) - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse colon tissue labeling MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1/500 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 AlexaFluor^® 488 Goat anti-Rabbit secondary at 1/1000 (2 μg/ml) dilution (Green). Positive staining on mouse colon is observed. The nuclear counterstain was DAPI (Blue).
  

  Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 AlexaFluor^® 488 Goat anti-Rabbit secondary at 1/1000 (2 μg/ml) 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-MUC2 antibody [EPR23479-47] ab272692).

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Immunohistochemical analysis of paraffin-embedded rat colon tissue labeling MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1/2000 dilution followed by ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Postive staining on rat colon is observed. The section was incubated with Anti-MUC2 antibody [EPR23479-47] ab272692 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND^® RX instrument. Counterstained with hematoxylin.
  

  Secondary antibody only control: Secondary antibody is ready to use 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 solution2) for 20 mins.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC2 antibody [EPR23479-47] ab272692).

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Immunohistochemical analysis of paraffin-embedded mouse colon tissue labeling MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1/2000 dilution followed by ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Postive staining on mouse colon is observed. The section was incubated with Anti-MUC2 antibody [EPR23479-47] ab272692 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND^® RX instrument. Counterstained with hematoxylin.
  

  Secondary antibody only control: Secondary antibody is a ready to use 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 solution2) for 20 mins.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC2 antibody [EPR23479-47] ab272692).

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Immunohistochemical analysis of paraffin-embedded human bladder cancer tissue labeling MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1/2000 dilution followed by ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Postive staining on human bladder cancer (PMID: 25197366). The section was incubated with Anti-MUC2 antibody [EPR23479-47] ab272692 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND^® RX instrument. Counterstained with hematoxylin.
  

  Secondary antibody only control: Secondary antibody is ready to use 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 solution2) for 20 mins.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC2 antibody [EPR23479-47] ab272692).

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Immunohistochemical analysis of paraffin-embedded human colon tissue labeling MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1/2000 dilution followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Postive staining on human colon (PMID: 28693267). The section was incubated with Anti-MUC2 antibody [EPR23479-47] ab272692 for 10 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND^® RX instrument. Counterstained with hematoxylin.
  

  Secondary antibody only control: Secondary antibody is ready to use 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 solution2) for 20 mins.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC2 antibody [EPR23479-47] ab272692).

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Fluorescence multiplex immunohistochemical analysis of the human jejunum (Formalin/PFA-fixed paraffin-embedded sections).
  
  Panel A: merged staining of anti-Muc2 (Anti-MUC2 antibody [EPR23479-47] ab272692, magenta; Opal™690), anti-Eph receptor B2 (Anti-Eph receptor B2 antibody [EPR22427-268] ab252935, green; Opal™520) and anti-ErbB3 / HER3 (Anti-ErbB3 / HER3 antibody [SP71] - BSA and Azide free ab236220, red; Opal™570) on human jejunum. Panel B: anti-Muc2 stained on goblet cells. Panel C: anti-Eph receptor B2 stained on intestinal stem and progenitor cells. Panel D: anti-ErbB3 / HER3 stained on epithelial cells. Opal Polymer HRP Ms + Rb was used as a secondary antibody.
  
  The section was incubated in three rounds of staining: in the order of Anti-MUC2 antibody [EPR23479-47] ab272692 at 1/2000 dilution (0.252 μg/ml), Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 at 1/1000 dilution  (0.527 μg/ml), and Anti-ErbB3 / HER3 antibody [SP71] - BSA and Azide free ab236220 at 1/3000 dilution (0.75 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. DAPI (blue) was used as a nuclear counter stain.
  
  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC2 antibody [EPR23479-47] ab272692).

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Fluorescence multiplex immunohistochemical analysis of the human colon (Formalin/PFA-fixed paraffin-embedded sections).
  
  Panel A: merged staining of anti-Muc2 (Anti-MUC2 antibody [EPR23479-47] ab272692, magenta; Opal™690), anti-Eph receptor B2 (Anti-Eph receptor B2 antibody [EPR22427-268] ab252935, green; Opal™520) and anti-ErbB3 / HER3 (Anti-ErbB3 / HER3 antibody [SP71] - BSA and Azide free ab236220, red; Opal™570) on human colon. Panel B: anti-Muc2 stained on goblet cells. Panel C: anti-Eph receptor B2 stained on intestinal stem and progenitor cells. Panel D: anti-ErbB3 / HER3 stained on epithelial cells. Opal Polymer HRP Ms + Rb was used as a secondary antibody.
  
  The section was incubated in three rounds of staining: in the order of Anti-MUC2 antibody [EPR23479-47] ab272692 at 1/2000 dilution (0.252 μg/ml), Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 at 1/1000 dilution  (0.527 μg/ml), and Anti-ErbB3 / HER3 antibody [SP71] - BSA and Azide free ab236220 at 1/3000 dilution (0.75 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. DAPI (blue) was used as a nuclear counter stain.
  
  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC2 antibody [EPR23479-47] ab272692).

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  MUC2 Multiplex immunohistochemistry staining of Rat small intestine tissue using rabbit Anti-MUC2 antibody

  This data was developed using Anti-MUC2 antibody [EPR23479-47] ab272692, the same antibody clone in a different buffer formulation.

  Immunohistochemistry analysis of Formalin/PFA-fixed paraffin-embedded sections rat small intestine tissue labelling Sodium/Hydrogen Exchanger 3 with Anti-Sodium/Hydrogen Exchanger 3/NHE-3 antibody [EPR26951-3] ab307365 at 1:5000 dilution (B), MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1:2000 dilution (C) Eph receptor B2 with Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 at 1:500 dilution (D). Opal Polymer HRP Ms + Rb was used as a secondary antibody, and
  DAPI was used for a nuclear counter stain. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  Panel A: merged staining of anti-Sodium/Hydrogen Exchanger 3 (green; Opal™520), anti-MUC2 (magenta; Opal™690) and anti-Eph receptor B2 (gray; Opal™570) on rat small intestine.

  Panel B: anti-Sodium/Hydrogen Exchanger 3 staining apical and luminal facing edges of surface cells in rat small intestine.

  Panel C: anti-MUC2 staining goblet cells in rat small intestine.

  Panel D: anti-Eph receptor B2 staining membrane of stem cells in rat small intestine.

  Nuclear DNA was labeled with DAPI (shown in blue).

  The section was incubated in three rounds of staining: in the order of Anti-Sodium/Hydrogen Exchanger 3/NHE-3 antibody [EPR26951-3] ab307365, Anti-MUC2 antibody [EPR23479-47] ab272692 and Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  Fluorescence multiplex immunohistochemical analysis of the human colon (Formalin/PFA-fixed paraffin-embedded sections). Panel A: merged staining of anti-Villin (Anti-Villin antibody [SP145] - BSA and Azide free ab245749, gray; Opal™690), anti-liver FABP (Anti-liver FABP antibody [EPR20464] - BSA and Azide free ab240401, green; Opal™520) and anti-MUC2 (Anti-MUC2 antibody [EPR23479-47] ab272692, red; Opal™570) on human colon. Panel B: anti-liver FABP stained on enterocytes. Panel C: anti-Villin stained on apical border. Panel D: anti-MUC2 stained on goblet cells. Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101) was used as a secondary antibody. The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. The section was incubated in three rounds of staining: in the order of Anti-Villin antibody [SP145] - BSA and Azide free ab245749 (1/1000 dilution), Anti-liver FABP antibody [EPR20464] - BSA and Azide free ab240401 (1/8000 dilution), and Anti-MUC2 antibody [EPR23479-47] ab272692 (1/5000 dilution) for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins. DAPI (blue) was used as a nuclear counter stain. Image acquisition was performed with Leica SP8 confocal microscope.
  
  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC2 antibody [EPR23479-47] ab272692).

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  MUC2 Multiplex immunohistochemistry staining of Rat colon tissue using rabbit Anti-MUC2 antibody

  This data was developed using Anti-MUC2 antibody [EPR23479-47] ab272692, the same antibody clone in a different buffer formulation.

  Immunohistochemistry analysis of Formalin/PFA-fixed paraffin-embedded sections rat colon tissue labelling Sodium/Hydrogen Exchanger 3 with Anti-Sodium/Hydrogen Exchanger 3/NHE-3 antibody [EPR26951-3] ab307365 at 1:5000 dilution (B), MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1:2000 dilution (C) Eph receptor B2 with Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 at 1:500 dilution (D). Opal Polymer HRP Ms + Rb was used as a secondary antibody, and
  DAPI was used for a nuclear counter stain. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  Panel A: merged staining of anti-Sodium/Hydrogen Exchanger 3 (green; Opal™520), anti-MUC2 (magenta; Opal™690) and anti-Eph receptor B2 (gray; Opal™570) on rat colon.

  Panel B: anti-Sodium/Hydrogen Exchanger 3 staining apical and luminal facing edges of surface cells in rat colon.

  Panel C: anti-MUC2 staining goblet cells in rat colon.

  Panel D: anti-Eph receptor B2 staining membrane of stem cells in rat colon.

  Nuclear DNA was labeled with DAPI (shown in blue).

  The section was incubated in three rounds of staining: in the order of Anti-Sodium/Hydrogen Exchanger 3/NHE-3 antibody [EPR26951-3] ab307365, Anti-MUC2 antibody [EPR23479-47] ab272692 and Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  MUC2 Multiplex immunohistochemistry staining of Mouse small intestine tissue using rabbit Anti-MUC2 antibody

  This data was developed using Anti-MUC2 antibody [EPR23479-47] ab272692, the same antibody clone in a different buffer formulation.

  Immunohistochemistry analysis of Formalin/PFA-fixed paraffin-embedded sections mouse small intestine tissue labelling Sodium/Hydrogen Exchanger 3 with Anti-Sodium/Hydrogen Exchanger 3/NHE-3 antibody [EPR26951-3] ab307365 at 1:5000 dilution (B), MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1:2000 dilution (C) Eph receptor B2 with Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 at 1:500 dilution (D). Opal Polymer HRP Ms + Rb was used as a secondary antibody, and
  DAPI was used for a nuclear counter stain. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  Panel A: merged staining of anti-Sodium/Hydrogen Exchanger 3 (green; Opal™520), anti-MUC2 (magenta; Opal™690) and anti-Eph receptor B2 (gray; Opal™570) on mouse small intestine.

  Panel B: anti-Sodium/Hydrogen Exchanger 3 staining apical and luminal facing edges of surface cells in mouse small intestine.

  Panel C: anti-MUC2 staining goblet cells in mouse small intestine.

  Panel D: anti-Eph receptor B2 staining membrane of stem cells in mouse small intestine.

  Nuclear DNA was labeled with DAPI (shown in blue).

  The section was incubated in three rounds of staining: in the order of Anti-Sodium/Hydrogen Exchanger 3/NHE-3 antibody [EPR26951-3] ab307365, Anti-MUC2 antibody [EPR23479-47] ab272692 and Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  MUC2 Multiplex immunohistochemistry staining of Mouse colon tissue using rabbit Anti-MUC2 antibody

  This data was developed using Anti-MUC2 antibody [EPR23479-47] ab272692, the same antibody clone in a different buffer formulation.

  Immunohistochemistry analysis of Formalin/PFA-fixed paraffin-embedded sections mouse colon tissue labelling Sodium/Hydrogen Exchanger 3 with Anti-Sodium/Hydrogen Exchanger 3/NHE-3 antibody [EPR26951-3] ab307365 at 1:5000 dilution (B), MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1:2000 dilution (C) Eph receptor B2 with Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 at 1:500 dilution (D). Opal Polymer HRP Ms + Rb was used as a secondary antibody, and
  DAPI was used for a nuclear counter stain. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  Panel A: merged staining of anti-Sodium/Hydrogen Exchanger 3 (green; Opal™520), anti-MUC2 (magenta; Opal™690) and anti-Eph receptor B2 (gray; Opal™570) on mouse colon.

  Panel B: anti-Sodium/Hydrogen Exchanger 3 staining apical and luminal facing edges of surface cells in mouse colon.

  Panel C: anti-MUC2 staining goblet cells in mouse colon.

  Panel D: anti-Eph receptor B2 staining membrane of stem cells in mouse colon.

  Nuclear DNA was labeled with DAPI (shown in blue).

  The section was incubated in three rounds of staining: in the order of Anti-Sodium/Hydrogen Exchanger 3/NHE-3 antibody [EPR26951-3] ab307365, Anti-MUC2 antibody [EPR23479-47] ab272692 and Anti-Eph receptor B2 antibody [EPR22427-268] ab252935 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  This data was developed using Anti-MUC2 antibody [EPR23479-47] ab272692, the same antibody clone in a different buffer formulation.
  

  Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human small intestine tissue staining MUC17 with Anti-MUC17 antibody [EPR28482-85] ab316971 at 1/500 dilution, Anti-MUC2 antibody [EPR23479-47] ab272692 anti-MUC2 used at 1/2000 dilution and Anti-REG1B antibody [EPR28864-4] ab323315 anti-REG1B used at a 1/5000 dilution. Opal Polymer HRP Ms + Rb was used as a secondary antibody, and DAPI was used for a nuclear counter stain. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  Panel A: merged staining of anti-MUC17 (green; Opal^™570), anti-MUC2 (magenta; Opal^™690) and anti-REG1B (grey; Opal^™520) on human small intestine.
  
  Panel B: anti-MUC17 staining epithelium in human small intestine.
  
  Panel C: anti-MUC2 staining goblet cells in human small intestine.
  
  Panel D: anti-REG1B staining Paneth cells in human small intestine.
  
  Nuclear DNA was labeled with DAPI (shown in blue).

  The section was incubated in three rounds of staining: in the order of Anti-MUC17 antibody [EPR28482-85] ab316971, Anti-MUC2 antibody [EPR23479-47] ab272692 and Anti-REG1B antibody [EPR28864-4] ab323315 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.

• 

  Multiplex immunohistochemistry - Anti-MUC2 antibody [EPR23479-47] - BSA and Azide free (ab272706)

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-MUC2 antibody [EPR23479-47] ab272692).

  Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Mouse colon tissue staining GSDMC2 + GSDMC3 with Anti-GSDMC2 + GSDMC3 antibody [EPR20890-48] ab229896 at a 1:2000 (0.25 ug/ml) dilution; SARM1 with Anti-SARM1 antibody [EPR24834-80] ab309195 at 1:500 (0.964 ug/ml) dilution and MUC2 with Anti-MUC2 antibody [EPR23479-47] ab272692 at 1:2000 (0.252 ug/ml) dilution followed by a ready to use secondary antibody Opal Polymer HRP Ms + Rb.

  Panel A: merged staining of anti-SARM1 (green; Opal^™520), anti-MUC2 (gray; Opal^™570) and anti-GSDMC2/3 (magenta; Opal^™690)on mouse colon.
  
  Panel B: anti-SARM1 staining myenteric nerve plexus in mouse colon.
  
  Panel C: anti-MUC2 staining goblet cells in mouse colon.
  
  Panel D: anti-GSDMC2/3 staining epithelium in mouse colon.
  
  Nuclear DNA was labeled with DAPI (shown in blue).

  The section was incubated in three rounds of staining: in the order of Anti-SARM1 antibody [EPR24834-80] ab309195, Anti-MUC2 antibody [EPR23479-47] ab272692 and Anti-GSDMC2 + GSDMC3 antibody [EPR20890-48] ab229896 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