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To determine protein expression, a 3D region of interest (ROI) was drawn over the injected muscle and ipsilateral popliteal LN and the maximum standard uptake value (SUVmax) of [18F]FP-TMP was quantified (Supplementary Fig. 2). E Uptake of [18F]FP-TMP in HEK293T cells transfected with S2PΔf-eDHFR or S2P mRNA. Recombinant spike S2 protein produced in insect cells was used as a positive management, 59 kDa. B LNPs transfect antigen-presenting cells (APCs) and mRNA is released and translated into S2PΔf-eDHFR. Co-incubation with a molar excess of unlabeled TMP abrogated uptake of [18F]FP-TMP, confirming specificity of our radiotracer for eDHFR (Fig. 1e). Cells transfected with S2P and S2PΔf-eDHFR demonstrated a rise in fluorescence compared with non-transfected cells suggesting floor expression of the S2PΔf-eDHFR fusion protein (Fig. 1d, Supplementary Fig. 1).<br>Nonetheless, the contribution of R p could additionally be considerable for high-energy positron emitters (e.g., 82Rb; ) and small-animal PET scanners (e.g., microPET system) having smaller detectors.The detailed technique of measuring the spatial resolution of a PET scanner is given later in this chapter. Two detectors detect these photons in a straight line, which is barely deviated from the original annihilation line. This error (R a) degrades the spatial decision of the scanner and deteriorates with the space between the two detectors. Thus, the observed LOR between the two detectors doesn't intersect the purpose of annihilation, but is somewhat displaced from it, as illustrated in Fig. The most deviation from the 180° direction is ±0.25° (i.e., 0.5° FWHM). 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