Fig. 10From: A cell death assay in barley and wheat protoplasts for identification and validation of matching pathogen AVR effector and plant NLR immune receptorsOverview of steps for protoplast recovery. Step 30: Up to six transfection samples tubes are centrifuged together at 1000 x g for 3 min. Step 31: Using a pipette, 965 µl of supernatant are remove from all transfection sample tubes. Step 32: 100 µl of 2× Cell Culture Lysis Buffer is transferred into each transfection sample tube. Step 33: Steps 30 to 32 are repeated for other transfection sample tubesBack to article page