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| [http://web.mit.edu/biology/sauerlab/ Official lab website]
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| =Lab members on OWW= | | =<font size=6 font style="color:#000000">Lab Information</font>= |
| [[User:Kathmc|Kathleen McGinness]]
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| [[Dan Bolon]] | | [[Sauer:Lab Members|<font size=4 font style="color:#000000">Lab Members</font>]] |
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| =Former lab members on OWW= | | [http://mit.edu/sauerlab/ <font size=4 font style="color:#000000">Official lab website</font>] |
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| [[User:Jimhu|Jim Hu]] | | [http://web.mit.edu/biology/www/facultyareas/facresearch/sauer.html <font size=4 font style="color:#000000">Bob Sauer's Department of Biology page</font>] |
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| =Protocols= | | =<font size=6 font style="color:#000000">Resources</font>= |
| Here we will post protocols that people in the lab generally use. Many of these will be lab-specific protocols, but if you think the protocol you are posting is more generally applicable, please link it to the general [[Protocols]] page. Also, if you typically do a variation of the protocol that is posted, please list it on the same page as a separate, alternative protocol. If possible, also try to note why what you do is different.
| | [[Sauer:Protocols|<font size=4 font style="color:#000000">Protocols</font>]] |
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| | [[Sauer:Links|<font size=4 font style="color:#000000">Links</font>]] |
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| '''PLEASE NOTE:''' Blindly following a protocol is not a good substitute for actually talking to someone who has done the experiment. When posting protocols, please also include the name(s) of people in the lab who will be good to talk to about the protocol.
| | [[Sauer:Internal|<font size=4 font style="color:#000000">Internal</font>]]</div> |
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| [[Sauer:ClpX purification]] | | <wikionly>[http://sauer.openwetware.org/ Dewikified version of the Sauer lab page]</wikionly> |
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| [[Sauer:ClpP purification]]
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| [[Sauer:In vitro degradation of GFP-ssrA by ClpXP]]
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| [[Sauer:Expression/purification of 35S-Met proteins]] | |
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| [[Sauer:In vitro degradation of radiolabeled proteins by ClpXP]]
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| [[Sauer:Western blot]]
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| [[Sauer:Quantitative Western blot]]
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| [[Sauer:Site-directed mutagenesis]]
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| [[Sauer:Competent cell preparation]]
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| =Equipment (Sauer lab)=
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| Please list here the equipment we have in our lab and the appropriate contact person for that piece of equipment. If it is something a lot of people use, also list other people that may be able to help out if there are any questions.
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| ==Thermocyclers (PCR machines)==
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| '''Located in room 565'''
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| Sign-up sheets for both machines are located nearby. Please use them, even if no one else is signed-up/using the machine. This lets people know where to put your reactions when they are finished if they need to use the machine, or who to talk to if they want to know when you're going to be finished.
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| *'''DNA engine'''
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| **Status quo set up has two independent blocks that can each hold up to 30 ~0.5 mL tubes
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| **We also have a gradient block (located on the shelf above the machine). This block holds one microtiter plate (96 well) or up to 96 0.2 mL tubes. You can set up a temperature gradient with this block to optimize your annealing temperature. To use this block, you need to remove the block with the two independent units and replace it with this one (turn the machine off first and ask someone/RTFM). Note that this means that no one else will be able to use the machine when you are using it, so please sign-up accordingly.
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| **Both blocks have a "hot top", so there is no need to use oil on top of your reaction.
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| *'''Perkin Elmer Cetus DNA thermal cycler 480'''
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| **affectionately referred to as "Bessie"
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| **This machine is an "old school" peltier thermal cycler. It holds up to 48 ~0.5 mL tubes. No hot top on this one, so be sure to use mineral oil on top of your reaction to prevent evaporation
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| =Equipment (other labs)=
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| Please list here equipment that we use in other labs along with a contact person in our lab and a contact person in the other lab. Tips on how reserving/using the equipment works would also be helpful i.e. do we need training on the equipment?.
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