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N. benthamiana plants were cultivated, infiltrated with A. tumefaciens and subsequently incubated as described before using either vacuum infiltration [39] or manual injection into leaves [27]. Whole plants or leaf discs were infiltrated with a bacterial suspension (OD600nm = 1.0) using infiltration buffer (0.5 g L−1 Fertilizer MEGA 2 (Planta Düngemittel GmbH, Regenstauf, Germany), 200 μM acetosyringone, pH 5.6). The infiltration buffer for PCPs additionally contained 50 g L−1 sucrose and 2 g L−1 glucose monohydrate. PCPs were generated from 300 μL of concentrated (200 g wet biomass L−1) continuously cultured BY-2 cells [40] and incubated in 96-well Agroprep Advance PP/PE 30–40 μm filter plates (Pall GmbH, Dreieich, Germany). |
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Protocol tips |
N. benthamiana plants were cultivated, infiltrated with A. tumefaciens and subsequently incubated as described before using either vacuum infiltration [39] or manual injection into leaves [27]. Whole plants or leaf discs were infiltrated with a bacterial suspension (OD600nm = 1.0) using infiltration buffer (0.5 g L−1 Fertilizer MEGA 2 (Planta Düngemittel GmbH, Regenstauf, Germany), 200 μM acetosyringone, pH 5.6). The infiltration buffer for PCPs additionally contained 50 g L−1 sucrose and 2 g L−1 glucose monohydrate. PCPs were generated from 300 μL of concentrated (200 g wet biomass L−1) continuously cultured BY-2 cells [40] and incubated in 96-well Agroprep Advance PP/PE 30–40 μm filter plates (Pall GmbH, Dreieich, Germany). |
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