Sentence examples for microscopy of donor from inspiring English sources

Fig. 1 Kelvin probe force microscopy of donor atoms.

This was established using confocal microscopy and immunohistochemical, or histochemical co-detection of donor and recipient markers in the same epithelial cell (Figure 1C-I and Figure S4A C).

Again, cell fusion was apparent in the DSS-induced colons of these animals by co-detection of donor and recipient markers using confocal microscopy (β-gal and GFP; Figure 2B D).

Post-transplantation analysis of the fate of donor cells was performed first by fluorescent microscopy at 4 and 6 weeks after injection.

The analysis of recipient testes by fluorescence microscopy at 1 and 14 h post-transplantation revealed the presence of donor germ cells in the lumen (Fig. 2a b) and in contact with recipient Sertoli cells (Fig. 2c d).

To quantitatively measure the interaction between EGFR eGFP and Grb2 mRFP in BaF/3 cells, we utilized lifetime-detected FRET FLIM microscopy, which enables a robust evaluation of FRET efficiency based on the quenching of donor lifetime in the presence of acceptor.

Expression of reporter proteins (GFP and DsRed) allowed in situ monitoring of donor cell attachment and plasmid transfer to the recipient cells using confocal laser scanning microscopy.

We examined the centrifuged platelets with transmission electron microscopy and confirmed that majority of cells, if not all, were platelets (data now shown due to a discrepancy of donor samples used for the study).

The presence of donor BMDCs in recipient mice was investigated in fat tissue vessels after DIO using in vivo and ex vivo fluorescence microscopy.

We then monitored the recruitment of donor T cells in the ankle joints and joint-draining lymph nodes of the recipients using in vivo two-photon microscopy and ex vivo detection methods.

(c) Confidentiality of donor information.