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Ntrifugation at 30,000 g for 5 h through a 10 -30 -60 sucrose-PBS step gradient. The virus band located at the 30 -60 sucrose interface was collected, titered, and stored at 80 . Soluble HSV glycoproteins and infected cell extracts used. Soluble gD1(306t) was produced in baculovirus-infected Sf9 cells and was purified as previously described (52). Cytoplasmic extracts of HSV-1(NS) (16)- or HSV-