Difference between revisions of "Part:BBa K649200:Experience"
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__NOTOC__ | __NOTOC__ | ||
===Applications of BBa_K649200=== | ===Applications of BBa_K649200=== | ||
− | + | In in vitro assay, the part was made linear using restriction enzymes. Cre recombinase was added to the linear DNA and incubated for 0.5, 2, and 4 hours. Images of the experiments have been added below.<br /> | |
− | + | '''[Sample]'''<br /> | |
+ | <table border="1"> | ||
+ | <tr> | ||
+ | <th>sample</th> | ||
+ | <th>volume</th> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>PlacIQ-lox2272-GFP-lox2272(pSB1C3)</td> | ||
+ | <td>50 ng/μl × 4 μl</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>10× Cre recombination Buffer</td> | ||
+ | <td>1 μl</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>ddH2O</td> | ||
+ | <td> 4 μl</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Cre recombinase</td> | ||
+ | <td>1,000 units/ml × 1 μl</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <th>total</th> | ||
+ | <th> 10 μl</th> | ||
+ | </tr> | ||
+ | </table> | ||
+ | |||
+ | |||
− | + | <br /> | |
+ | '''[Method]''' | ||
+ | 1. The part on pSB1C3 was made linear by EcoRV restriction site which is far from lox sites. <br /> | ||
+ | 2. Three identical samples and one negative control without Cre-recombinase had been prepared and those were incubated in 37°C for 0.5hr, 2hr and 4hr respectively. Negative control was incubated for 4hr.<br /> | ||
+ | 3. After a period of time, the samples were kept in -20°C until the whole samples are arranged. The result was checked by electrophoresis(0.8% EtBr(+) agarose gell, 100V, 400mA, 30min) | ||
+ | |||
===User Reviews=== | ===User Reviews=== |
Revision as of 08:41, 4 October 2011
Applications of BBa_K649200
In in vitro assay, the part was made linear using restriction enzymes. Cre recombinase was added to the linear DNA and incubated for 0.5, 2, and 4 hours. Images of the experiments have been added below.
[Sample]
sample | volume |
---|---|
PlacIQ-lox2272-GFP-lox2272(pSB1C3) | 50 ng/μl × 4 μl |
10× Cre recombination Buffer | 1 μl |
ddH2O | 4 μl |
Cre recombinase | 1,000 units/ml × 1 μl |
total | 10 μl |
[Method]
1. The part on pSB1C3 was made linear by EcoRV restriction site which is far from lox sites.
2. Three identical samples and one negative control without Cre-recombinase had been prepared and those were incubated in 37°C for 0.5hr, 2hr and 4hr respectively. Negative control was incubated for 4hr.
3. After a period of time, the samples were kept in -20°C until the whole samples are arranged. The result was checked by electrophoresis(0.8% EtBr(+) agarose gell, 100V, 400mA, 30min)
User Reviews
UNIQc741d790b2c5f2c8-partinfo-00000000-QINU UNIQc741d790b2c5f2c8-partinfo-00000001-QINU