Figure 1
Figure 1. Detection of Neu5Gc in aortic endothelium of human autopsy samples and microvasculature of colon and placenta. The chicken anti-Neu5Gc antibody (cGcAb) was used to detect the presence of Neu5Gc on the endothelium of autopsy samples of normal-appearing human aorta. Typical representatives of 8 autopsy samples studied are shown. The red Cy3 fluorescence represents labeling of endothelial cells of the aorta. (A) Specificity of the antibody was demonstrated by the lack of signal with the nonimmunized control chicken IgY (middle) and the abrogation of signal by adsorption with Neu5Gc-rich glycoproteins of chimpanzee serum (right). Magnification ×200. (B) Sections were double-stained with anti-CD31 for endothelial cells and counterstained with DAPI to visualize nuclei (magnification ×1000). (C) Sections of placenta (top) and colon (bottom) stain for Neu5Gc along microvasculature endothelial lining with the use of cGcAb. Control IgY (right) demonstrates specificity of signal (magnification ×200).

Detection of Neu5Gc in aortic endothelium of human autopsy samples and microvasculature of colon and placenta. The chicken anti-Neu5Gc antibody (cGcAb) was used to detect the presence of Neu5Gc on the endothelium of autopsy samples of normal-appearing human aorta. Typical representatives of 8 autopsy samples studied are shown. The red Cy3 fluorescence represents labeling of endothelial cells of the aorta. (A) Specificity of the antibody was demonstrated by the lack of signal with the nonimmunized control chicken IgY (middle) and the abrogation of signal by adsorption with Neu5Gc-rich glycoproteins of chimpanzee serum (right). Magnification ×200. (B) Sections were double-stained with anti-CD31 for endothelial cells and counterstained with DAPI to visualize nuclei (magnification ×1000). (C) Sections of placenta (top) and colon (bottom) stain for Neu5Gc along microvasculature endothelial lining with the use of cGcAb. Control IgY (right) demonstrates specificity of signal (magnification ×200).

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