Briefly, tissue pieces (2mm×5mm) were excised from roots of salt stressed and unstressed plants and then vacuum infiltrated with freshly prepared 5mM CeCl3 in 50mM 3-(N-morpholino)-propanesulfonic acid at pH7.2 for 30 min.
Briefly, tissue pieces (2mm×5mm) were excisedfrom roots of salt stressed and unstressed plants and then vacuum infiltrated with freshly prepared 5mM CeCl3 in 50mM3-(N-morpholino)-propanesulfonic acid at pH7.2 for 30 min.