4.5.1. alamarBlueTM Assay

AA Anna-Klara Amler
PD Patrick H. Dinkelborg
DS Domenic Schlauch
JS Jacob Spinnen
SS Stefan Stich
RL Roland Lauster
MS Michael Sittinger
SN Susanne Nahles
MH Max Heiland
LK Lutz Kloke
CR Carsten Rendenbach
BB Benedicta Beck-Broichsitter
TD Tilo Dehne
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To evaluate cell viability after printing, alamarBlueTM assay was used according to the manufacturer’s recommendations (Thermo Fisher Scientific, Waltham, MA, USA). AlamarBlueTM was diluted 1:10 in DMEM containing 10% FCS (AB medium). The medium was removed and each construct was incubated in 500 μL AB medium for 4 h at 37 °C and 5% CO2. After the incubation period, 4 × 100 μL of each well was transferred to a 96-well plate. Fluorescence was measured in a plate reader with the following wavelength filter settings—540 nm for excitation and 590 nm for emission. AB medium without any cells served as a blank measurement. Two bioprinted constructs per condition were analyzed and measured in technical quadruplicates.

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