Anti-GPCR GPR17 antibody [EPR26423-34]

37 product images

• 

  Multiplex immunohistochemistry - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  GPCR GPR17 Multiplex immunohistochemistry staining of Human cerebrum tissue using rabbit Anti-GPCR GPR17 antibody

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded human cerebrum tissue sections.
  

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-TMEM119 (green; Opal™520) and anti-GFAP (red; Opal™570) on human cerebrum.

  Panel B: anti-GPR17 staining oligodendrocytes in human cerebrum.

  Panel C: anti-TMEM119 staining microglia in human cerebrum.

  Panel D: anti-GFAP staining astrocytes in human cerebrum.

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-TMEM119 antibody [EPR25865-89] - Microglial marker ab306583 at a 1/2000 dilution, and Anti-GFAP antibody [EPR1034Y] - BSA and Azide free ab218309 at a 1/1000 dilution for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Nuclear counterstaining with DAPI.

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

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  GPCR GPR17 Multiplex immunohistochemistry staining of Mouse cerebrum tissue using rabbit Anti-GPCR GPR17 antibody

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse cerebrum tissue sections.
  

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-GFAP (red; Opal™570) on mouse cerebrum.

  Panel B: anti-GPR17 staining oligodendrocytes in mouse cerebrum.

  Panel C: anti-P2RY12 staining microglia in mouse cerebrum.

  Panel D: anti-GFAP staining astrocytes in mouse cerebrum.

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/140000 dilution, and Anti-GFAP antibody [EPR1034Y] - BSA and Azide free ab218309 at a 1/1000 dilution for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Nuclear counterstaining with DAPI.

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

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  GPCR GPR17 Multiplex immunohistochemistry staining of Rat cerebrum tissue using rabbit Anti-GPCR GPR17 antibody

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded rat cerebrum tissue sections.
  

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-GFAP (red; Opal™570) on rat cerebrum.

  Panel B: anti-GPR17 staining oligodendrocytes in rat cerebrum.

  Panel C: anti-P2RY12 staining microglia in rat cerebrum.

  Panel D: anti-GFAP staining astrocytes in rat cerebrum.

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/140000 dilution, and Anti-GFAP antibody [EPR1034Y] - BSA and Azide free ab218309 at a 1/1000 dilution for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Nuclear counterstaining with DAPI.

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

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  GPCR GPR17 Multiplex immunohistochemistry staining of Mouse cerebellum tissue using rabbit Anti-GPCR GPR17 antibody

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse cerebellum tissue sections.

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-GFAP (red; Opal™570) on mouse cerebellum.

  Panel B: anti-GPR17 staining oligodendrocytes in mouse cerebellum.

  Panel C: anti-P2RY12 staining microglia in mouse cerebellum.

  Panel D: anti-GFAP staining astrocytes in mouse cerebellum.

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution, and Anti-GFAP antibody [EPR1034Y] - BSA and Azide free ab218309 at a 1/1000 dilution for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  Nuclear counterstaining with DAPI.

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

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  GPCR GPR17 Multiplex immunohistochemistry staining of Mouse hippocampus tissue using rabbit Anti-GPCR GPR17 antibody

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse hippocampus tissue sections.

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-GFAP (red; Opal™570) on mouse hippocampus.

  Panel B: anti-GPR17 staining oligodendrocytes in mouse hippocampus.

  Panel C: anti-P2RY12 staining microglia in mouse hippocampus.

  Panel D: anti-GFAP staining astrocytes in mouse hippocampus.

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000, and Anti-GFAP antibody [EPR1034Y] - BSA and Azide free ab218309 at a 1/1000 dilution for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  Nuclear counterstaining with DAPI.

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

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  GPCR GPR17 Multiplex immunohistochemistry staining of Mouse spinal cord tissue using rabbit Anti-GPCR GPR17 antibody

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse spinal cord tissue sections.

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-GFAP (red; Opal™570) on mouse spinal cord.

  Panel B: anti-GPR17 staining oligodendrocytes in mouse spinal cord.

  Panel C: anti-P2RY12 staining microglia in mouse spinal cord.

  Panel D: anti-GFAP staining astrocytes in mouse spinal cord.

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution, and Anti-GFAP antibody [EPR1034Y] - BSA and Azide free ab218309 at a 1/1000 dilution for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  Nuclear counterstaining with DAPI.

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

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  GPCR GPR17 Multiplex immunohistochemistry staining of Rat spinal cord tissue using rabbit Anti-GPCR GPR17 antibody

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded rat spinal cord tissue sections.

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-GFAP (red; Opal™570) on rat spinal cord.

  Panel B: anti-GPR17 staining oligodendrocytes in rat spinal cord.

  Panel C: anti-P2RY12 staining microglia in rat spinal cord.

  Panel D: anti-GFAP staining astrocytes in rat spinal cord.

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution, and Anti-GFAP antibody [EPR1034Y] - BSA and Azide free ab218309 at a 1/1000 dilution for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  Nuclear counterstaining with DAPI.

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

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded rat spinal cord tissue staining Mu Opioid Receptor with Anti-Mu Opioid Receptor antibody [EPR29112-126] ab323645 at a 1:2000 (0.252 ug/ml) dilution, Anti-TAC1 antibody [EPR26567-18-1-3] ab307138 anti-TAC1 used at 1:500 (0.966 ug/ml) dilution and ab316105 anti-GPCR GPR17 used at a 1:500 (0.509ug/ml) dilution.

  Panel A: merged staining of anti-OPRM1 (magenta; Opal™520), anti-TAC1 (green; Opal™690) and anti-GPCR GPR17 (yellow; Opal™570) on rat spinal cord.
  
  Panel B: anti-OPRM1 showed positive staining in rat spinal cord.
  
  Panel C: anti-TAC1 showed positive staining in rat spinal cord.
  
  Panel D: anti-GPCR GPR17 staining oligodendrocytes in rat spinal cord.
  
  Nuclear DNA was labeled with DAPI (shown in blue).

  The section was incubated in three rounds of staining: in the order of Anti-Mu Opioid Receptor antibody [EPR29112-126] ab323645, Anti-TAC1 antibody [EPR26567-18-1-3] ab307138 and ab316105 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  Nuclear counter stain with DAPI.

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

• 

  Multiplex immunohistochemistry - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse spinal cord tissue staining Mu Opioid Receptor with Anti-Mu Opioid Receptor antibody [EPR29112-126] ab323645 at a 1:2000 (0.252 ug/ml) dilution, Anti-TAC1 antibody [EPR26567-18-1-3] ab307138 anti-TAC1 used at 1:500 (0.966 ug/ml) dilution and ab316105 anti-GPCR GPR17 used at a 1:500 (0.509ug/ml) dilution.

  Panel A: merged staining of anti-OPRM1 (magenta; Opal™520), anti-TAC1 (green; Opal™690) and anti-GPCR GPR17 (yellow; Opal™570) on mouse spinal cord.
  
  Panel B: anti-OPRM1 showed positive staining in mouse spinal cord.
  
  Panel C: anti-TAC1 showed positive staining in mouse spinal cord.
  
  Panel D: anti-GPCR GPR17 staining oligodendrocytes in mouse spinal cord.
  
  Nuclear DNA was labeled with DAPI (shown in blue).

  The section was incubated in three rounds of staining: in the order of Anti-Mu Opioid Receptor antibody [EPR29112-126] ab323645, Anti-TAC1 antibody [EPR26567-18-1-3] ab307138 and ab316105 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.

  Nuclear counter stain with DAPI.

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

• 

  Multiplex immunohistochemistry - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse cerebellum tissue sections.

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-FMR1 (gray; Opal™570) on mouse cerebellum.

  Panel B: anti-GPR17 staining oligodendrocytes in mouse cerebellum.

  Panel C: anti-P2RY12 staining microglia in mouse cerebellum.

  Panel D: anti-FMR1 staining neurons and Purkinje cells in mouse cerebellum.

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

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution and Anti-FMRP antibody [EPR23852-90] ab259335 at a 1/10000 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.

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse cerebrum tissue sections.
  

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-FMR1 (gray; Opal™570) on mouse cerebrum.

  Panel B: anti-GPR17 staining oligodendrocytes in mouse cerebrum.

  Panel C: anti-P2RY12 staining microglia in mouse cerebrum.

  Panel D: anti-FMR1 staining neurons in mouse cerebrum.

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

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution, and Anti-FMRP antibody [EPR23852-90] ab259335 at a 1/10000 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.

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse hippocampus tissue sections.
  

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-FMR1 (gray; Opal™570) on mouse hippocampus.

  Panel B: anti-GPR17 staining oligodendrocytes in mouse hippocampus.

  Panel C: anti-P2RY12 staining microglia in mouse hippocampus.

  Panel D: anti-FMR1 staining neurons in mouse hippocampus.

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

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution, and Anti-FMRP antibody [EPR23852-90] ab259335 at a 1/10000 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. Nuclear counterstaining with DAPI.

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded rat cerebrum tissue sections.

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-FMR1 (gray; Opal™570) on rat cerebrum.

  Panel B: anti-GPR17 staining oligodendrocytes in rat cerebrum.

  Panel C: anti-P2RY12 staining microglia in rat cerebrum.

  Panel D: anti-FMR1 staining neurons in rat cerebrum.

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

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution, and Anti-FMRP antibody [EPR23852-90] ab259335 at a 1/10000 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. Nuclear counterstaining with DAPI.

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded rat hippocampus tissue sections.

  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-FMR1 (gray; Opal™570) on rat hippocampus.

  Panel B: anti-GPR17 staining oligodendrocytes in rat hippocampus.

  Panel C: anti-P2RY12 staining microglia in rat hippocampus.

  Panel D: anti-FMR1 staining neurons in rat hippocampus.

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

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution, and Anti-FMRP antibody [EPR23852-90] ab259335 at a 1/10000 dilution for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Nuclear counterstaining with DAPI.

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

  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-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Fluorescence multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse spinal cord tissue.

  
  Panel A: merged staining of anti-GPR17 (magenta; Opal™690), anti-P2RY12 (green; Opal™520) and anti-FMR1 (gray; Opal™570) on mouse spinal cord.
  
  Panel B: anti-GPR17 staining oligodendrocytes in mouse spinal cord.
  
  Panel C: anti-P2RY12 staining microglia in mouse spinal cord.
  
  Panel D: anti-FMR1 staining neurons in mouse spinal cord.
  
  Nuclear DNA was labeled with DAPI (shown in blue).
  

  The section was incubated in three rounds of staining: in the order of ab316105 at a 1/500 dilution, Anti-P2Y12 antibody [EPR26298-93] ab300140 at a 1/40000 dilution, and Anti-FMRP antibody [EPR23852-90] ab259335 at a 1/10000 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.

  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.

• 

  Flow Cytometry (Intracellular) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Mouse primary neuron cells labelling GPCR GPR17 with ab316105 at 1/500 dilution (0.1 ug)/Right compared with a Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) / Left isotype control.

  Goat Anti-Rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081) at 1/5000 dilution was used as the secondary antibody.

• 

  Flow Cytometry (Intracellular) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Isotype (Left) / 293T (human embryonic kidney epithelial cell) transfected with an empty expression vector containing a myc tag (Middle) / 293T transfected with a GPCR expression vector containing a myc tag (Right) cells labelling GPCR GPR17 with ab316105 at 1/500 dilution (0.1 ug)/Middle and Right compared with a Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) / Left isotype control.

  Goat Anti-Rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081) at 1/5000 dilution was used as the secondary antibody.

  Cells are co-stained with Myc tag conjugated to Alexa Fluor®647.

• 

  Immunohistochemistry (Frozen sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse liver (fresh frozen) tissue labeling GPCR GPR17 with ab316105 at 1/50 (10.18 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).

  Negative control: confocal image showing no staining on mouse liver. The nuclear counterstain was DAPI (Blue). The section was incubated with ab316105 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.

• 

  Immunohistochemistry (Frozen sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebellum (fresh frozen) tissue labeling GPCR GPR17 with ab316105 at 1/50 (10.18 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).

  Confocal image showing positive staining on mouse cerebellum. The nuclear counterstain was DAPI (Blue). The section was incubated with ab316105 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.

• 

  Immunohistochemistry (Frozen sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebellum (fresh frozen) tissue labeling GPCR GPR17 with ab316105 at 1/50 (10.18 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed ab150088 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed ab150088) at 1/1000 (2 ug/mL) dilution (Green).

  Panel A: merged staining of anti-GPCR GPR17 (ab316105, green), anti-Olig2 (Alexa Fluor® 488 Anti-Olig2 antibody [EPR2673] ab225099, red) and anti-GFAP (Alexa Fluor® 647 Anti-GFAP antibody [EPR1034Y] - Mouse IgG1 Chimeric ab313596, grey) on mouse cerebellum.
  
  Panel B: anti-GPCR GPR17 stained on mouse cerebellum.
  
  Panel C: anti-Olig2 stained in oligodendrocyte of mouse cerebellum.
  
  Panel D: anti-GFAP stained in astrocytes of mouse cerebellum.
  
  The nuclear counterstain was DAPI (Blue). The section was incubated with ab316105 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed ab150088 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed ab150088)at 1/1000 (2 ug/mL) dilution.

• 

  Immunohistochemistry (Frozen sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat liver (fresh frozen) tissue labeling GPCR GPR17 with ab316105 at 1/50 (10.18 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).

  Negative control: confocal image showing no staining on rat liver (PMID: 16990797). The nuclear counterstain was DAPI (Blue). The section was incubated with ab316105 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.

• 

  Immunohistochemistry (Frozen sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat cerebellum (fresh frozen) tissue labeling GPCR GPR17 with ab316105 at 1/50 (10.18 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).

  Confocal image showing positive staining on rat cerebellum. The nuclear counterstain was DAPI (Blue). The section was incubated with ab316105 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.

• 

  Immunohistochemistry (Frozen sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat cerebellum (fresh frozen) tissue labeling GPCR GPR17 with ab316105 at 1/50 (10.18 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed ab150088 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed ab150088) at 1/1000 (2 ug/mL) dilution (Green).

  Panel A: merged staining of anti-GPCR GPR17 (ab316105, green), anti-Olig2 (Alexa Fluor® 488 Anti-Olig2 antibody [EPR2673] ab225099, red) and anti-GFAP (Alexa Fluor® 647 Anti-GFAP antibody [EPR1034Y] - Mouse IgG1 Chimeric ab313596, grey) on rat cerebellum.
  
  Panel B: anti-GPCR GPR17 stained on rat cerebellum.
  
  Panel C: anti-Olig2 stained in oligodendrocyte of rat cerebellum.
  
  Panel D: anti-GFAP stained in astrocytes of rat cerebellum.
  
  The nuclear counterstain was DAPI (Blue). The section was incubated with ab316105 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed ab150088 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) preadsorbed ab150088)at 1/1000 (2 ug/mL) dilution.

• 

  Immunocytochemistry/ Immunofluorescence - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized rat primary neural/glia cell cells labelling GPCR GPR17 with ab316105 at 1/50 (10.18 ug/ml) dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/mL) dilution (Green).

  Confocal image showing cytoplasmic staining in rat oligodendrocytes.
  
  Confocal scanning Z step was set as 0.3 ?m followed by image processing with maximum Z projection.
  
  Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8).

  Anti-MAP2 antibody [HM-2] - Neuronal Marker ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain at 1/500 (4 ug/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).

  Secondary antibody only control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution.

• 

  Immunocytochemistry/ Immunofluorescence - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse primary neural/glia cell cells labelling GPCR GPR17 with ab316105 at 1/50 (10.18 ug/ml) dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/mL) dilution (Green).

  Confocal image showing cytoplasmic staining in mouse oligodendrocytes.
  
  Confocal scanning Z step was set as 0.3 ?m followed by image processing with maximum Z projection.
  
  Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8).

  Anti-MAP2 antibody [HM-2] - Neuronal Marker ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain at 1/500 (4 ug/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).

  Secondary antibody only control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution.

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded (A) HEK-293T (human epithelial cell line from embryonic kidney) transfected with a GPR17 expression vector containing a Myc-His tag. (B) HEK-293T transfected with empty vector containing a Myc-His tag. tissue labeling GPCR GPR17 with ab316105 at 1/5000 (0.102 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

  Positive staining on (A) HEK-293T (human epithelial cell line from embryonic kidney) transfected with a GPR17 expression vector containing a Myc-His tag, negative staining on (B) HEK-293T transfected with empty vector containing a Myc-His tag. The section was incubated with ab316105 for 30 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 LeicaDS9800 (Bond™ Polymer Refine Detection).

  Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Rat cardiac muscle tissue labeling GPCR GPR17 with ab316105 at 1/2000 (0.255 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

  Negative control: no staining on rat cardiac muscle. The section was incubated with ab316105 for 30 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling GPCR GPR17 with ab316105 at 1/2000 (0.255 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

  Negative control: no staining on rat liver (PMID: 16990797). The section was incubated with ab316105 for 30 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Mouse cardiac muscle tissue labeling GPCR GPR17 with ab316105 at 1/2000 (0.255 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

  Negative control: no staining on mouse cardiac muscle. The section was incubated with ab316105 for 30 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling GPCR GPR17 with ab316105 at 1/2000 (0.255 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

  Negative control: no staining on mouse liver. The section was incubated with ab316105 for 30 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling GPCR GPR17 with ab316105 at 1/500 (1.018 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

  Negative control: no staining on human liver (PMID: 16990797). The section was incubated with ab316105 for 30 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling GPCR GPR17 with ab316105 at 1/2000 (0.255 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

  Positive staining on oligodendrocytes of rat cerebrum (PMID: 21209081). The section was incubated with ab316105 for 30 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 LeicaDS9800 (Bond™ Polymer Refine Detection).

  Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling GPCR GPR17 with ab316105 at 1/2000 (0.255 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

  Positive staining on oligodendrocytes of mouse cerebrum (PMID: 26453964). The section was incubated with ab316105 for 30 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 LeicaDS9800 (Bond™ Polymer Refine Detection).

  Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling GPCR GPR17 with ab316105 at 1/500 (1.018 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

  Positive staining on oligodendrocytes of human cerebrum (PMID: 28357182; PMID: 23801362). The section was incubated with ab316105 for 30 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

• 

  Immunoprecipitation - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  GPCR GPR17 was immunoprecipitated from 0.35 mg Mouse brain tissue lysate with ab316105 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab316105 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.

  Lane 1: Mouse brain tissue lysate
  
  Lane 2: ab316105 IP in Mouse brain tissue lysate
  
  Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of ab316105 in mouse brain tissue lysate.

  All lanes: Immunoprecipitation - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105) at 1/30 dilution

  All lanes: Mouse brain tissue lysate with 5% NFDM/TBST

  Secondary

  All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution

  Exposure time: 180s

• 

  Western blot - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Negative control: heart, lung and spleen(PMID: 19625605), (PMID: 19838178).

  In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.

  All lanes: Western blot - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105) at 1/1000 dilution

  Lane 1: Mouse P14 spinal cord tissue lysate at 40 µg with 5% NFDM/TBST

  Lane 2: Mouse P14 brain tissue lysate at 40 µg with 5% NFDM/TBST

  Lane 3: Mouse heart tissue lysate at 40 µg with 5% NFDM/TBST

  Lane 4: Mouse lung tissue lysate at 40 µg with 5% NFDM/TBST

  Lane 5: Mouse spleen tissue lysate at 40 µg with 5% NFDM/TBST

  Lane 6: Rat P14 spinal cord tissue lysate at 40 µg with 5% NFDM/TBST

  Lane 7: Rat P14 brain tissue lysate at 40 µg with 5% NFDM/TBST

  Lane 8: Rat heart tissue lysate at 40 µg with 5% NFDM/TBST

  Secondary

  All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

  Observed band size: 40 kDa, 36 kDa

  Exposure time: 103s

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPCR GPR17 antibody [EPR26423-34] (ab316105)

  Immunohistochemical analysis of paraffin-embedded Human cardiac muscle tissue labeling GPCR GPR17 with ab316105 at 1/500 (1.018 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

  Negative control: no staining on human cardiac muscle. The section was incubated with ab316105 for 30 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins