User:Daniel-Mario Larco/Notebook/AU Photosynthesis Lab/2014/07/14: Difference between revisions
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==SDS-PAGE== | ==SDS-PAGE== | ||
#Our protein solution was collected from the cold room and transferred into a 50mL falcon tube | #Our protein solution was collected from the cold room and transferred into a 50mL falcon tube labeled Purified Hb pH7, 7/14/14 | ||
#We will run a gel with the solution and past solution to check purity | #We will run a gel with the solution and past solution to check purity | ||
#The gel will be set up in the following order | #The gel will be set up in the following order | ||
##Myoglobin and BSA ladder | ##Myoglobin and BSA ladder | ||
##Empty | ##Empty | ||
## | ##Protein in pH8.3 tris (solution that was injected into Q-Sepharose column) | ||
## | ##Elute during injection of Protein in pH8.3 tris into Q-Sepharose column | ||
## | ##Elute during cleaning Q-Sepharose column containing Protein in pH8.3 tris with 1M NaCl | ||
## | ##Elute from SP-Sepharose column in phosphate buffer pH7.2 during injection (from fractions collected from Q-Sepharose column) | ||
## | ##Empty | ||
## | ##1/10 dilution of Ammonium sulfate treatment pellet dissolved in 50mM Tris | ||
## | ##1/10 dilution of purified protein from dialysis over the weekend | ||
## | ##1/100 dilution of purified protein from dialysis over the weekend | ||
## | ##Empty | ||
## | ##Myoglobin and BSA ladder | ||
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Revision as of 06:27, 14 July 2014
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