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Team:Macquarie Australia/Protocols/SDSPAGE
From 2012.igem.org
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<center><h1>SDS-PAGE</h1></center> | <center><h1>SDS-PAGE</h1></center> | ||
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| - | Pelleted cells were resuspended in 200 uL Milli-Q H2O. | + | <center>Pelleted cells were resuspended in 200 uL Milli-Q H2O. </center> <br> |
| - | Transferred 50 uL of suspension into new Eppendorf tubes and combined with 50 uL 2x TruSep sample buffer. | + | <center>Transferred 50 uL of suspension into new Eppendorf tubes and combined with 50 uL 2x TruSep sample buffer. </center><br> |
| - | Using a Hamilton syringe, the cells were sheared. | + | <center>Using a Hamilton syringe, the cells were sheared. </center><br> |
| - | Centrifuged the preparations for 3 mins @ 13,000 rpm. | + | <center>Centrifuged the preparations for 3 mins @ 13,000 rpm.</center> <br> |
| - | Loaded 20 uL of the supernatant in to the gel. | + | <center>Loaded 20 uL of the supernatant in to the gel. </center> <br> |
| + | <center>Electrophoresis was conducted at constant voltage (200 V) for one hour. </center> <br> | ||
Latest revision as of 03:54, 27 September 2012
SDS-PAGE
