Confluent HFF cells were treated with irradiation of 55 Gy and plated
onto culture dishes (1 × 105 per 2.89 cm2).
Not exact matches
A swab of a patient's bladder cells were
cultured in a
dish, molded to the shape of the bladder, and tacked
onto their original damaged organ, restoring function.
After 6 — 7 days of suspension
culture, the neurospheres were replated
onto matrigel - coated 60 mm tissue
culture dishes for adherent
culture in the same medium for another 2 — 3 days.
Primary neurospheres were then collected and replated
onto matrigel - coated tissue
culture dishes for adherent
culture in the same medium for another 2 — 3 days.
Labelled outer segments were washed, resuspended in human foetal RPE medium and seeded
onto iPS - RPE cells
cultured on gelatin - coated 35 mm
dishes.