Haynes Lab:Notebook/Engineering PC-TFs/2013/03/02

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(Autocreate 2013/03/02 Entry for Haynes_Lab:Notebook/Engineering_PC-TFs)
(Summary)
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==Summary==
==Summary==
-
*  
+
* Retrieve mini preps for flyPCD assembly from freezer and thaw at room temperature.
 +
* Also let restriction enzymes thaw.
 +
 
 +
*Do restriction digest (EcoRI/PstI)''Diagnostic digest''
 +
 
 +
{| {{table}}
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| align="center" style="background:#f0f0f0;"|''''''
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| align="center" style="background:#f0f0f0;"|''''''
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| align="center" style="background:#f0f0f0;"|'''15 µl Total'''
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| align="center" style="background:#f0f0f0;"|'''Master Mix'''
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|-
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| ||||1 rxn||x 9
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|-
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| DNA plasmid||||3||--
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|-
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| enzyme 1||||1||9
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|-
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| enzyme 2||||1||9
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|-
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| 10x buffer||||1.5||13.5
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|-
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| dH2O||||8.5||76.5
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|-
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|
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|}
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*Aliquot 12 μL to each tube. Then add 3 μL DNA to each tube.
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*Place each tube in heat block 37°C.
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Follow steps for gel electrophoresis.
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*  Orient top notch of gel electrophoresis apparatus. Place gel tray into larger tray.
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*  Fill gel flask with up to 60 ml of TA buffer.
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*  Create 1% gel by putting .6 grams of agarose into flask.
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*  Microwave agarose solution for 40 seconds
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*  Using hot gloves, grab flask out of microwave and swirl flask vigorously. Place back in microwave for 40 more seconds.
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*  When flask is taken out of microwave, make sure that the agarose is completed dissolved.
 +
*  Set up wells on gel electrophoresis apparatus. The mold for the first digest is B-10. Use the thick "teeth" and slip in the notches.
 +
*  Add EtBr (ethidium bromide) to the agarose gel. There should be 1 microliter of EtBr per 10ml of agarose gel. Therefore, 6 µL.
 +
*  Pour gel into tray.
 +
*  Wash the agarose gel flask.

Revision as of 20:59, 2 March 2013

Engineering PC-TFs Main project page
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Summary

  • Retrieve mini preps for flyPCD assembly from freezer and thaw at room temperature.
  • Also let restriction enzymes thaw.
  • Do restriction digest (EcoRI/PstI)Diagnostic digest
' ' 15 µl Total Master Mix
1 rxnx 9
DNA plasmid3--
enzyme 119
enzyme 219
10x buffer1.513.5
dH2O8.576.5
  • Aliquot 12 μL to each tube. Then add 3 μL DNA to each tube.
  • Place each tube in heat block 37°C.

Follow steps for gel electrophoresis.

  • Orient top notch of gel electrophoresis apparatus. Place gel tray into larger tray.
  • Fill gel flask with up to 60 ml of TA buffer.
  • Create 1% gel by putting .6 grams of agarose into flask.
  • Microwave agarose solution for 40 seconds
  • Using hot gloves, grab flask out of microwave and swirl flask vigorously. Place back in microwave for 40 more seconds.
  • When flask is taken out of microwave, make sure that the agarose is completed dissolved.
  • Set up wells on gel electrophoresis apparatus. The mold for the first digest is B-10. Use the thick "teeth" and slip in the notches.
  • Add EtBr (ethidium bromide) to the agarose gel. There should be 1 microliter of EtBr per 10ml of agarose gel. Therefore, 6 µL.
  • Pour gel into tray.
  • Wash the agarose gel flask.



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