To detect regulatory T cells, we co-stained our sections
by immunofluorescence for FoxP3 and CD4 - expressing cells.
Not exact matches
The HepG2 cells were treated with ActD
for 6 h, and the p53 expression level was examined
by immunofluorescence imaging.
After binding, cells were washed once (carefully using a 200 μl pipette to remove the medium) with RPMI with 0.5 % BSA solution and adherent cells were analyzed
by immunofluorescence microscopy or bright field microscopy
for quantification.
All cases were analysed
for IgA anti-gliadin (AGA)
by an ELISA test and those with positive results were tested
for IgA anti-endomysium antibody (EMA) using
immunofluorescence.