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. 2009 Jan;149(1):412–423. doi: 10.1104/pp.108.127761

Figure 8.

Figure 8.

Stability and intracellular transport of LMW-GS in tobacco protoplasts. A, Protoplasts were transfected with vector alone (vector) or constructs encoding either the B11-33-HA or the C(25, 230)S-HA protein, labeled for 1 h with [35S]Cys and [35S]Met and then chased for the times indicated. Proteins were immunoselected from cell homogenates with anti-HA antibodies and analyzed by reducing SDS-PAGE and fluorography. B, Protoplasts were transfected and pulse-labeled as in A and then chased for the times indicated. After fractionation into a membrane and a soluble fraction as in “Materials and Methods,” proteins were immunoselected with anti-HA or anti-BiP antibodies and analyzed by reducing SDS-PAGE and fluorography. The arrowhead indicates the position of the BiP polypeptide.