840:153g:Projects/project23/2012/10/25
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==Continuation of the Mutagenesis Reaction == | ==Continuation of the Mutagenesis Reaction == | ||
| - | * On Tuesday, we ran the gel for last week's PCR products. | + | * On Tuesday, we ran the gel for last week's PCR products. The high concentration of 1:20 template DNA, and a low concentration of 1:200 were prepared with water for each the upstream and downstream fragments. Our nomenclature used is three-part, and outlined below. |
| + | *1.)Primer configuration | ||
| + | **N = no primers used | ||
| + | **P = outside primers used | ||
| + | *2.)Template DNA concentration | ||
| + | ** + = 1:20 | ||
| + | ** - = 1:200 | ||
| + | *3.)Annealing temperature for PCR, in °C | ||
| + | |||
| + | |||
| + | *Our positive control was standard template DNA and associated primers from lab stock | ||
| + | *Our negative control had outside primers and no template | ||
| + | |||
| + | |||
| + | *We loaded our samples as follows: | ||
*Top Lane: | *Top Lane: | ||
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#N+60 | #N+60 | ||
#N+65 | #N+65 | ||
| - | # | + | #Negative Control |
#N-55 | #N-55 | ||
#N-60 | #N-60 | ||
Revision as of 18:14, 29 October 2012
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Continuation of the Mutagenesis Reaction
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