Lan:LE daily entries: Difference between revisions

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*'''Experimental procedures:''' Refer to appropriate protocol and note any changes in them
*'''Experimental procedures:''' Refer to appropriate protocol and note any changes in them
*'''Results:''' Post pictures with caption and appropriate identification of lanes on gels
*'''Results:''' Post pictures with caption and appropriate identification of lanes on gels
State what are your finding and any comments
**State what are your finding and any comments


<h1>2008/06/30 - AP06-39</h1>
<h1>2008/06/30 - AP06-39</h1>
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Digestion positives clone(ND01-XX and ND01-YY) where tested for protein expression
Digestion positives clone(ND01-XX and ND01-YY) where tested for protein expression
<h3>Experimental procedures</h3>
<h3>Experimental procedures</h3>
* Used O/N culture for miniprep to inoculate 10 mL 2XYTGB flasks(125 mL)to OD~0.4
* Used O/N culture for miniprep to inoculate 10 mL 2XYTGB flasks(125 mL) to OD~0.4
* Induced with 0.1 mM IPTG (100 µL of 100 mM stock)
* Induced with 0.1 mM IPTG (100 µL of 100 mM stock)
* Incubated in shaker B at 37°C O/N
* Incubated in shaker B at 37°C O/N
* Harvested at 7:30 and lysed using lysis buffer (10X stock diluted to 1X, nothing else)
* Harvested at 7:30 and lysed using lysis buffer (10X stock diluted to 1X, nothing else)
<h3>Results</h3>
<h3>Results</h3>

Revision as of 06:51, 29 June 2008

Please follow this format for your entries

  • Date(year/month/day)-Hard copy lab book reference (Initials lab book #-page)
  • Title of experiment with brief description
  • Experimental procedures: Refer to appropriate protocol and note any changes in them
  • Results: Post pictures with caption and appropriate identification of lanes on gels
    • State what are your finding and any comments

2008/06/30 - AP06-39

Expression assay on positives clones

Digestion positives clone(ND01-XX and ND01-YY) where tested for protein expression

Experimental procedures

  • Used O/N culture for miniprep to inoculate 10 mL 2XYTGB flasks(125 mL) to OD~0.4
  • Induced with 0.1 mM IPTG (100 µL of 100 mM stock)
  • Incubated in shaker B at 37°C O/N
  • Harvested at 7:30 and lysed using lysis buffer (10X stock diluted to 1X, nothing else)

Results