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Products:Immunology >> Innate Immunity >> Macrophage / Inflamm.
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Read our guarantee »Anti-Monocyte + Macrophage antibody [MOMA-2]
See all Monocyte + Macrophage products (5) ...
Rat monoclonal [MOMA-2] to Monocyte + Macrophage
This antibody recognises an intracellular antigen of mouse macrophages and monocytes. It reacts strongly with macrophages in lymphoid organs in all mouse strains tested. Staining may also be seen on the epithelium of mucosa.
IHC-FoFr, Flow Cyt, IHC-Frmore details
Reacts with
Mouse
Mouse lymph node stroma
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: 0.09% Sodium Azide
Concentration information loading...
Protein G purified
Monoclonal
MOMA-2
IgG2b
Immunohistochemistry (PFA perfusion fixed frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)
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Immunohistochemistry (Frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)
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Immunohistochemistry (Frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)
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Our Abpromise guarantee covers the use of ab33451 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-FoFr: 1/50.
Flow Cyt: Use at an assay dependent dilution. Membrane permeabilisation is required for this application.
IHC-Fr: 1/25.
Monocyte and macrophage are white blood cells that roam the body tissues engulfing foreign organisms. A monocyte is a leukocyte, part of the human body's immune system that protects against blood-borne pathogens and moves quickly (aprox. 8-12 hours) to sites of infection in the tissues. Monocytes are usually identified in stained smears by their large bi-lobed nucleus. Macrophages are cells within the tissues that originate from specific white blood cells called monocytes. Monocytes and macrophages are phagocytes, acting in both nonspecific defense (or innate immunity) as well as specific defense (or cell-mediated immunity) of vertebrate animals. Their role is to phagocytize (engulf and then digest) cellular debris and pathogens either as stationary or mobile cells, and to stimulate lymphocytes and other immune cells to respond to the pathogen.
Immunohistochemistry (PFA perfusion fixed frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)
![Immunohistochemistry (PFA perfusion fixed frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)](/ps/datasheet/Images/33/ab33451/ab33451_1.jpg)
ab33451 staining mouse brain tissue sections by IHC-FoFr. Sections were PFA fixed and blocked with 0.5% TNB for 30 minutes at 25°C. The primary antibody was diluted 1/50 and incubated with the sample for 18 hours at 4°C. A HRP conjugated goat anti-rat antibody, diluted 1/500, was used as the secondary.
This antibody labels perivascular (left) and subpial (right) macs in normal brain tissue.
This image is courtesy of an anonymous Abreview
Immunohistochemistry (Frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)
![Immunohistochemistry (Frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)](/ps/datasheet/images/33/ab33451/Monocyte-Macrophage-Primary-antibodies-ab33451-1.jpg)
ab33451 staining Monocyte + Macrophage in mouse suprarenal aorta sections by Immunohistonchemistry (Frozen sections).Serial cryostat sections 7 µm thick were cut from suprarenal aortas with aneurysms prior to staining for inflammatory cells. Serial frozen sections were air-dried, fixed in acetone for 10 minutes at -20°C, air dried and rehydrated with PBS before being incubated in 3% H2O2/0.1% sodium azide/PBS to block endogenous peroxidase. For macrophage detection, sections were blocked in 2% normal goat serum in PBS followed by staining using ab33451. Slides were incubated in the peroxidase substrate 3, 3'-diamminobenzidine, counterstained in Mayer's Haematoxylin, dehydrated, cleared in xylene and mounted in Depex mounting medium.
Image from Rush C et al, BMC Genomics. 2009 Jul 6;10:298, Fig 3.
Immunohistochemistry (Frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)
![Immunohistochemistry (Frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)](/ps/datasheet/images/33/ab33451/Monocyte-Macrophage-Primary-antibodies-ab33451-6.jpg)
ab33451 staining Monocyte + Macrophage in Mouse aorta tissue by Immunohistochemistry (Frozen sections). The sections were fixed in acetone prior to blocking with 5% serum for 30 minutes at room temperature. The primary antibody was diluted 1/50 in PBS and incubated with the sample for 1 hour. A FITC-conjugated Rabbit anti-Rat polyclonal was used as the secondary antibody, diluted 1/400.
Endothelium is stained with Von Willebrand Factor (ab6994) and counterstained with DAPI
This image is courtesy of an anonymous Abreview.
This product has been referenced in:
See all 6 publications for this product
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![Immunohistochemistry (PFA perfusion fixed frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)](/ps/datasheet/Images/33/ab33451/ab33451_1.jpg)
ab33451 staining mouse brain tissue sections by IHC-FoFr. Sections were PFA fixed and blocked with 0.5% TNB for 30 minutes at 25°C. The primary antibody was diluted 1/50 and incubated with the sample for 18 hours at 4°C. A HRP conjugated goat anti-rat antibody, diluted 1/500, was used as the secondary.
This antibody labels perivascular (left) and subpial (right) macs in normal brain tissue.
This image is courtesy of an anonymous Abreview
![Immunohistochemistry (Frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)](/ps/datasheet/images/33/ab33451/Monocyte-Macrophage-Primary-antibodies-ab33451-1.jpg)
ab33451 staining Monocyte + Macrophage in mouse suprarenal aorta sections by Immunohistonchemistry (Frozen sections).Serial cryostat sections 7 µm thick were cut from suprarenal aortas with aneurysms prior to staining for inflammatory cells. Serial frozen sections were air-dried, fixed in acetone for 10 minutes at -20°C, air dried and rehydrated with PBS before being incubated in 3% H2O2/0.1% sodium azide/PBS to block endogenous peroxidase. For macrophage detection, sections were blocked in 2% normal goat serum in PBS followed by staining using ab33451. Slides were incubated in the peroxidase substrate 3, 3'-diamminobenzidine, counterstained in Mayer's Haematoxylin, dehydrated, cleared in xylene and mounted in Depex mounting medium.
Image from Rush C et al, BMC Genomics. 2009 Jul 6;10:298, Fig 3.
![Immunohistochemistry (Frozen sections) - Monocyte + Macrophage antibody [MOMA-2] (ab33451)](/ps/datasheet/images/33/ab33451/Monocyte-Macrophage-Primary-antibodies-ab33451-6.jpg)
ab33451 staining Monocyte + Macrophage in Mouse aorta tissue by Immunohistochemistry (Frozen sections). The sections were fixed in acetone prior to blocking with 5% serum for 30 minutes at room temperature. The primary antibody was diluted 1/50 in PBS and incubated with the sample for 1 hour. A FITC-conjugated Rabbit anti-Rat polyclonal was used as the secondary antibody, diluted 1/400.
Endothelium is stained with Von Willebrand Factor (ab6994) and counterstained with DAPI
This image is courtesy of an anonymous Abreview.
![Anti-Monocyte + Macrophage antibody [MOMA-2] for Immunohistochemistry (Frozen sections) in Mouse (33451)](/ps/datasheet/images/33/ab33451/Monocyte-Macrophage-Primary-antibodies-ab33451-9.jpg)
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