Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Mouse liver tissue sections labeling F4/80 with ab111101 at 1/250 dilution (0.48 µg/ml). Heat mediated antigen retrieval using ab93684 (Tris/EDTA buffer, pH 9.0). Goat Anti-Rabbit IgG H&L (HRP) was used as the secondary antibody. Hematoxylin was used as a counterstain. Positive staining on macrophages in the mouse liver. This image was generated using ab111101, the same clone, but with a different buffer formulation.

Representative immunostaining of F4/80-positive macrophages in the distal colon from healthy and colitic mice treated with and without enoxaparin.

For immunohistochemical staining, antigen retrieval was performed by incubating the sections for 10 minutes at 97°C in 1 mM EDTA buffer, pH 8 or 10 mM citrate buffer, pH 6. Activity of endogenous peroxidase was blocked by incubating sections with 3% v/v hydrogen for 20 minutes. Sections were then washed with 0.05 M Tris-buffered saline containing 0.5% v/v Tween 20 (TBST), pH 7.6. Subsequently, sections were incubated with serum-free protein block for 10 minutes. Colon sections were then incubated with primary antibody ab111101 at 1/100 dilution overnight at 4°C or room temperature for 1 hour. Sections were then washed 3 x 5 minutes and allowed to react with secondary antibody: anti-rabbit immunoglobulin C conjugated to horseradish peroxidase (HRP) (ab7090) at 1/300 dilution at room temperature for 1 hour.

Scale bar = 100 μm for 400 x magnification. Control, C; untreated colitis, DSS; oral enoxaparin, OE; intraperitoneal injection of enoxaparin, IPE.

This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA and sodium azide (ab111101).

Representative images of (A) M1 macrophages (F4/80⁺ and iNOS⁺) and (B) M2 macrophages (F4/80⁺ and CD206⁺) using colon tissue from n = 3–5 mice. F4/80 positive cells were visualized using Alexa Fluor 594-conjugated goat anti-rat IgG (red). Nuclei were stained with 4’,6-diamidino-2-phenylindole (DAPI, blue).

Scale bar = 50 μm for 400 × magnification. Control, C; untreated colitis, DSS; colitis with oral enoxaparin, DSS+OE.

For immunofluorescence staining, sections were dewaxed and rehydrated before antigen retrieval using 10 mM citrate buffer, pH 6 for 15 minutes at 97°C. Sections were incubated with serum-free protein block and permeabilized with 0.4% v/v Triton-X at room temperature for 30 minutes. Sections were incubated with primary antibodies anti-F4/80 (ab16911) at 1/25 dilution overnight at 4°C or at room temperature for 1 hour. Sections were washed with TBST 3 × 10 minutes and incubated with species-specific secondary antibodies: anti-rat IgG H&L AlexaFluor 594 (ab150160, Abcam, 1:1000) and anti-rabbit IgG H&L AlexaFluor 488 (A11070{"type":"entrez-nucleotide","attrs":{"text":"A11070","term_id":"490922","term_text":"A11070"}}, Thermo Fisher Scientific, Melbourne, Australia, 1:1000) at room temperature for 2 hours. Sections were rinsed with TBST 3 × 10 minutes, followed by a quick wash with distilled water before mounting using Glycerol Mounting Medium (Abcam) that contained 4’,6-diamidino-2-phenylindole (DAPI) and 1,4-diazobicyclo-2,2,2-octane (DABCO). Labelled tissues were visualized using a Leica DM LB2 microscope. Fluorescence images (400 × magnification) were captured using NIS-Elements 4.13 (Nikon) software. 

For full image see PMID: 26218284.

This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA and sodium azide (ab111101).

Immunohistochemical analysis staining for macrophages in (A) mouse uterus and (B) mouse spleen using ab111101 at a dilution of 1:200. HRP Anti-Rabbit IgG (Peroxidase) Polymer D antibody was used as a secondary. 

This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA and sodium azide (ab111101).

ab111101 at 1/100 dilution staining F4/80 in Formalin-fixed, paraffin-embedded Mouse liver tissue.

This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA and sodium azide (ab111101).

This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA and sodium azide (ab111101).