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Tc 4000 Para Rfactor 16
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transmission electron microscopy of cell wall ultrathin sections. hypernukleation is characterized by pathological accumulation of tau proteins in post-mitotic cell types and their anatomical connections. in contrast, in normal neurons, tau proteins are not observed at all, and are only found at the axon terminal as a presynaptic cytoskeletal protein.
transmission electron microscopy of cell wall ultrathin sections. hypernukleation is characterized by pathological accumulation of tau proteins in post-mitotic cell types and their anatomical connections. in contrast, in normal neurons, tau proteins are not observed at all, and are only found at the axon terminal as a presynaptic cytoskeletal protein.
e. coli cells were grown aerobically in ty medium until the od600 reached 0.3. the cells were harvested by centrifugation at 8000g for 10min, washed twice with mm and then divided into two 1l aliquots. one aliquot was treated with 20mm edta to remove the outer membrane and the other aliquot was treated with 20mm fecl2 to initiate haem incorporation. both aliquots were then incubated with shaking for 30min at 25°c and then spun for 20min at 4°c. the membranes were collected by ultracentrifugation at 200,000g for 1h and then the pellets were washed twice in ice-cold m-mem. the harvested membranes were resuspended in m-mem and stored at -80°c for at least 3months. the membrane protein aliquots were diluted in sample buffer [124mm trishcl, ph7.0, 20% glycerol, 4.6% sodium dodecyl sulphate (sds) and 50mm 2-mercaptoethanol] and incubated at room temperature for 10min.
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