840:153g:Projects/project22/2012/11/08: Difference between revisions
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==Gel Electrophoresis and PCR Setup== | ==Gel Electrophoresis and PCR Setup== | ||
* Upon our second extraction, we have been able to isolate DNA. We know this because on Tuesday we ran gel electrophoresis and had very bright bands that correspond with DNA. Today, we digested our samples and ran them through another gel to determine if they were digestible (using EcoR1). We did see a size difference between digested and undigested samples (lanes 13,15 and 17 were undigested and lanes 12, 14 and 16 were digested), except for in sample 3, which was in lanes 12 and 13. Lane 12 did not produce a band at all, and lane 13 produced an abnormal band ('streakier' than our other digested samples. | * Upon our second extraction, we have been able to isolate DNA. We know this because on Tuesday we ran gel electrophoresis and had very bright bands that correspond with DNA. Today, we digested our samples and ran them through another gel to determine if they were digestible (using EcoR1). We did see a size difference between digested and undigested samples (lanes 13,15 and 17 were undigested and lanes 12, 14 and 16 were digested), except for in sample 3, which was in lanes 12 and 13. Lane 12 did not produce a band at all, and lane 13 produced an abnormal band ('streakier' than our other digested samples). | ||
[[Image:Small_gel_11.08.12.png]] <-- Note the differences in lanes 12 and 13 from lanes 14-17 | [[Image:Small_gel_11.08.12.png]] <-- Note the differences in lanes 12 and 13 from lanes 14-17 |
Revision as of 21:58, 8 November 2012
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Gel Electrophoresis and PCR Setup
<-- Note the differences in lanes 12 and 13 from lanes 14-17
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