Mouse Monoclonal Endothelium, macrophages and red blood cells antibody. Carrier free. Suitable for Flow Cyt, IHC-Fr and reacts with Rat samples.
Constituents: PBS
Flow Cyt | IHC-Fr | |
---|---|---|
Rat | Tested | Tested |
Species | Dilution info | Notes |
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Species Rat | Dilution info 0.2 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1 µg/mL | Notes - |
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Mouse Monoclonal Endothelium, macrophages and red blood cells antibody. Carrier free. Suitable for Flow Cyt, IHC-Fr and reacts with Rat samples.
Constituents: PBS
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This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
The endothelium macrophages and red blood cells form an essential network within the circulatory system. The endothelium lines the interior surface of blood vessels playing an important role in vascular biology. Macrophages present in the blood as well as tissues act in innate immunity by engulfing pathogens and debris. Red blood cells carry oxygen from the lungs to the body tissues and return carbon dioxide from tissues to the lungs. The macrophages in blood known as blood macrophages are distinguished by markers such as CD14 and CD68 and can be analyzed using flow cytometry techniques. Understanding these cells is fundamental in immunology and hematological studies.
The endothelium forms a selective barrier that regulates the exchange of substances between the bloodstream and surrounding tissues. Macrophages on the other hand are versatile cells involved in inflammation tissue repair and immune responses. They secrete cytokines and chemokines that recruit other immune cells to the site of infection or injury. Endothelium and macrophages interact dynamically influencing vascular tone and response to inflammation. The red blood cells lacking a nucleus optimize oxygen transport due to their biconcave shape and high hemoglobin content around 270 million molecules per cell.
Endothelium and macrophages participate actively in the inflammatory response and coagulation pathways. The nitric oxide pathway for example involves endothelium-derived nitric oxide which relaxes vascular smooth muscle and regulates blood pressure. Macrophages generate inflammatory mediators like TNF-alpha and interleukin-6 components of the cytokine signaling pathway that modulate immune responses. Both cell types relate to proteins such as intercellular adhesion molecule-1 (ICAM-1) on endothelial cells facilitating leukocyte transmigration during immune surveillance and inflammation.
Endothelium dysfunction and macrophage activation relate closely to atherosclerosis and systemic inflammatory disorders. Atherosclerosis involves lipid accumulation in arterial walls where endothelial cells and macrophages contribute to plaque formation. Red blood cells can aggravate this process if they hemolyze within plaques. Disorders like rheumatoid arthritis feature aberrant activation of both endothelium and macrophages leading to chronic inflammation. Proteins such as VCAM-1 and E-selectin expressed on endothelial cells are associated with these vascular and systemic inflammatory diseases highlighting their role in cell adhesion and recruitment of immune cells.
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This data was developed using the same antibody clone in a different buffer formulation (Anti-Endothelium, macrophages and red blood cells antibody [OX-43] ab243850)
Lewis rat bone marrow cells stained with Anti-Endothelium, macrophages and red blood cells antibody [OX-43] ab243850 (right) or mouse IgG1κ (Mouse IgG1, kappa monoclonal [15-6E10A7] - Isotype Control ab170190) isotype (left). Lewis rat bone marrow cells were incubated for 30 min on ice in 1x PBS / 10 % rat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (Anti-Endothelium, macrophages and red blood cells antibody [OX-43] ab243850) or mouse IgG1κ (Mouse IgG1, kappa monoclonal [15-6E10A7] - Isotype Control ab170190) (1x106 in 100 μl at 0.2 μg/ml) for 30 min on ice.
The secondary antibody Goat anti-mouse IgG H&L (Alexa Fluor ® 488, pre-adsorbed) (Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed ab150117) was used at 1/2000 dilution for 30 min on ice. The cells were simultaneously stained with Ter-119 antibody.
Acquisition of >30,000 events were collected using a 50 mW Blue laser (488nm) and 530/30 bandpass filter. Events were gated on viable cells
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (Anti-Endothelium, macrophages and red blood cells antibody [OX-43] ab243850).
IHC image of Endothelium, macrophages and red blood cells staining in a section of frozen normal Rat Lung.
The section was fixed using 10% formaldehyde in 1XPBS for 10 minutes. No antigen retrieval step was performed prior to staining. Non-specific protein-protein interactions were then blocked in TBS containing 0.025% (v/v) Triton X-100, 0.3M glycine and 1% (w/v) BSA for 1h at room temperature. The section was then incubated overnight at +4°C in TBS containing 0.025% (v/v) Triton X-100 and 1% (w/v) BSA with Anti-Endothelium, macrophages and red blood cells antibody [OX-43] ab243850 at 1μg/ml. The section was then incubated with Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed ab150117 (Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preabsorbed, (Shown in green) 1/1000) for 1 hour at room temperature. DAPI was used to stain the cell nuclei (blue). The secondary-only control insert image is taken from an identical assay without primary antibody. The section was then mounted using Fluoromount®.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
For IHC staining systems (automated and non-automated), customers should optimize variable parameters such as antibody concentrations and incubation times.
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