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. Author manuscript; available in PMC: 2014 Jun 20.
Published in final edited form as: Lab Chip. 2009 Feb 4;9(10):1357–1364. doi: 10.1039/b818813k

Fig. 2.

Fig. 2

Representative images of cells captured from erythrocyte lysed blood onto antibody spots under static incubation conditions. The antibodies used are (a) anti-CD14 clone MY4, (b) anti-CD14 clone RMO52, (c) anti-CD14 clone UCHM1 and (d) anti-CD36 clone SMO. After rinsing off unbound cells, the cells captured on the antibody spots were stained using FITC-anti-CD36 (green), PE-anti-CD14 (red) and DAPI (blue). The images were created by overlapping the fluorescence photographs. The triple stained cells are monocytes, CD36 + CD14− cells are likely platelets and CD36−CD14+ cells are likely neutrophils. From the images, anti-CD14 MY4 clone and RMO52 clone captures monocytes efficiently, while anti-CD36 captures mostly platelets. (Scale bars: 100 μm).