Journal: Sensors and Actuators B: Chemical
Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates
doi: 10.1016/j.snb.2024.136939
Figure Lengend Snippet: Fig. 6. Schematic representation of recapture experiment on ExoView R100 (upper panel) and relative high resolution close ups of a Probe2 spot throughout experimental stages (bottom panel). From left to the right it can be seen i) the surface of the DNA spot, ii) label free interferometry picture of EVs captured on the same spot, and iii) red and green fluorescence picture of the same spot after incubation with labeled antibodies. The bar graphs represent label free interferometric and fluorescent detection of EVs on DNA microarray after separation using streptavidin coated magnetic beads: (b) functionalized with antiCD9-Tag2; (c) func- tionalized with Rabbit IgG-Tag2; (d) non functionalized with AACs. As additional negative control, detection of plasma added with antiCD9-Tag2 without previous separation of EVs on magnetic beads (e). Mean ± standard deviation of three independent measurements.
Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.
Techniques: Fluorescence, Incubation, Labeling, Microarray, Magnetic Beads, Negative Control, Clinical Proteomics, Standard Deviation