User:Tara K. Luckau/Notebook/Team ConGen/2011/03/04: Difference between revisions
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==Scun22 Optimization PCR Gel== | ==Scun22 Optimization PCR Gel== | ||
* from 23 february 2011 PCR (full temperature and buffer gradient) | * from 23 february 2011 PCR (full temperature and buffer gradient) | ||
===Gel Specs=== | |||
* Pour: 270mL 1xTAE + 5g agarose (supposed to have been 5.4g) + 27µL GelRed | * Pour: 270mL 1xTAE + 5g agarose (supposed to have been 5.4g) + 27µL GelRed | ||
* Run: 40 min @ 110V | * Run: 40 min @ 110V | ||
===Gel Images=== | |||
* [[Image:20110304_Row1.TIF|750 px]] | |||
* [[Image:20110304_Row2.TIF|750 px]] | |||
* [[Image:20110304_Row3.TIF|750 px]] | |||
* Only Buffer G yielded any product ... zoom in: | |||
* [[Image:20110304a_Row3Right.jpg|750 px]] | |||
===Conclusions=== | |||
* doesn't look like a typical MgCl<sub>2</sub> and temperature gradient PCR | |||
* inconsistent banding patterns across temperatures with dropouts | |||
* regardless, there is mispriming in all conditions that yielded any product | |||
* <span style="background:#7CFC00">Scun22 might not be a primer that will work for Sceloporus occidentalis</span> | |||
__NOTOC__ | __NOTOC__ |
Revision as of 17:22, 4 March 2011
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Scun22 Optimization PCR Gel
Gel Specs
Gel Images
Conclusions
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