VirusInfectionofFibroblasts
Procedure: Day One 1. Plate cells in 60 mm dishes using 5 ml DMEM containing 10% Calf Serum. The protocol has worked well for NIH3T3 with 1 x 105 cells and BALB/c3T3 with 2 x 105 cells. For the NIH cell line use 10% fetal calf serum and for the BALB cells use 10% calf serum.2. Grow cells overnight under appropriate conditions.Day Two1. Thaw virus stocks at 37°C and as soon as it has thawed transfer to ice b......阅读全文
Virus-Infection-of-Fibroblasts
Procedure: Day One 1. Plate cells in 60 mm dishes using 5 ml DMEM containing 10% Calf Serum. The protocol has worked well for NIH3T3 with 1 x 105 c
Virus-Infection-of-Fibroblasts
Procedure: Day One 1. Plate cells in 60 mm dishes using 5 ml DMEM containing 10% Calf Serum. The protocol has worked well for NIH3T3 with 1 x 105 c
Infection-with-retroviruses
It is well established with avian retroviruses that cells are most efficiently infected just after they are trypsinized. Trypsinization does two thin
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You will need:13.5 day pregnant mouse (we use MTK NEO inbred white mice)2 sets sterile instrumentsone containing a pair of curved forceps and a pair o
LentiVirus-Protocol
Lenti-Virus Protocol张端午A. For packing virus in 6-well plate: (if in 12-well plate, reduce all to 1/2)1. Mix the following plasmids in a 1.5 ml eppendo
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1. Adventitia from the main pulmonary artery was harvested neonatal calves. 2. Tissue was collected, carefully dissected free of blood vessels and f
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Creation and use of your infectious vector:Plate 5 x 105 293T cells in 6 cm2 dishes containing 5 ml of media. (This can be scaled up if desired).The f
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