Cellular MG quantification

MN Marie-Julie Nokin
FD Florence Durieux
PP Paul Peixoto
BC Barbara Chiavarina
OP Olivier Peulen
AB Arnaud Blomme
AT Andrei Turtoi
BC Brunella Costanza
NS Nicolas Smargiasso
DB Dominique Baiwir
JS Jean L Scheijen
CS Casper G Schalkwijk
JL Justine Leenders
PT Pascal De Tullio
EB Elettra Bianchi
MT Marc Thiry
KU Koji Uchida
DS David A Spiegel
JC James R Cochrane
CH Craig A Hutton
EP Edwin De Pauw
PD Philippe Delvenne
DB Dominique Belpomme
VC Vincent Castronovo
AB Akeila Bellahcène
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MBo (Methyl diaminobenzene-BODIPY) was used to detect endogenous MG in different conditions. The cells were treated with 5 µM MBo in complete medium as previously described (Wang et al., 2013). After 1 hr, the cells were washed with PBS and incubated in low- or high-glucose medium for 6 (FACS) and 24 hr (confocal microscopy). Cells were either trypsinized and analyzed by flow cytometry (BD Biosciences FACSCanto), or fixed with PAF and prepared for confocal microscope visualization as described above.

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