User:NYOUSHA Yousefi/Notebook/Protein Engineering/2012/10/09
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==Procedure== | ==Procedure== | ||
| - | #The containers frozen cells were taken out of the freezer and were allowed to slowly cool down at the room temperature in a beaker full of tap water. | + | #The zinc protoporphyrin prepared in previous labs was presented to cultured cells. |
| - | #When the cells mixture completely turned into liquid, | + | #The containers of the frozen cells were taken out of the freezer and were allowed to slowly cool down at the room temperature in a beaker full of tap water. |
| - | #The cell mixtures were placed into special centrifuge tubes and their weights were balanced to | + | #When the cells mixture completely turned into liquid, the cells were killed and broken apart by a ultrasound processor in 30seconds intervals of ultrasound and 30s intervals of sitting still in the ice. This intervals were repeated for 3 times. |
| + | #The cell mixtures were placed into special centrifuge tubes and their weights were balanced to three decimal places. | ||
#The cells were centrifuges at 18000g for two hours. | #The cells were centrifuges at 18000g for two hours. | ||
#After the centrifuge, the supernatant was separated and stored in different tubes. | #After the centrifuge, the supernatant was separated and stored in different tubes. | ||
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Entry titleProtein expression ObjectiveThe frozen cells, that were presented with Zn Hb and were allowed to replicate, were prepared for further protein expression studies Procedure
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