Fig. 1.
Fig. 1. eALAS protein synthesis in different erythroid tissues. / Peripheral blood and bone marrow were diluted with DMEM without methionine to 3 mL, separated on 3 mL Ficoll-Hypaque gradients, resuspended in 1 mL medium (blood, 1.5 × 108 cells; bone marrow, 1.9 × 107 cells), and incubated with 7.4 MBq (200 μCi) 35S-methionine for 3 hours. Detergent lysates were prepared, and eALAS and gel separation were immunoprecipitated. The arrows indicate the presumed pre-eALAS, the 59-kd form, and the herein described 52-kd eALAS-short.

eALAS protein synthesis in different erythroid tissues.

Peripheral blood and bone marrow were diluted with DMEM without methionine to 3 mL, separated on 3 mL Ficoll-Hypaque gradients, resuspended in 1 mL medium (blood, 1.5 × 108 cells; bone marrow, 1.9 × 107 cells), and incubated with 7.4 MBq (200 μCi) 35S-methionine for 3 hours. Detergent lysates were prepared, and eALAS and gel separation were immunoprecipitated. The arrows indicate the presumed pre-eALAS, the 59-kd form, and the herein described 52-kd eALAS-short.

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