Difference between revisions of "Part:BBa K2719004:Experience"
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===Applications of BBa_K2719004=== | ===Applications of BBa_K2719004=== | ||
<p>This part was optimized <i>Escherichia coli</i> BL21 (DE3) so it could be transformed into it and also cloned in pSB1C3. For proving it presence it was necessary to make two agarose gels, one for the entire plasmid and the other one for the restriction part in order to observe the insert. (Figure 2)</p> | <p>This part was optimized <i>Escherichia coli</i> BL21 (DE3) so it could be transformed into it and also cloned in pSB1C3. For proving it presence it was necessary to make two agarose gels, one for the entire plasmid and the other one for the restriction part in order to observe the insert. (Figure 2)</p> | ||
| + | [[file:T--TecCEM--TCSD5Colonies.png|500px]] | ||
| + | <p><i>Figure 1.</i> Colonies transformed with Tenascin Fibronectin domains.</p> | ||
===User Reviews=== | ===User Reviews=== | ||
Revision as of 16:51, 17 October 2018
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K2719004
This part was optimized Escherichia coli BL21 (DE3) so it could be transformed into it and also cloned in pSB1C3. For proving it presence it was necessary to make two agarose gels, one for the entire plasmid and the other one for the restriction part in order to observe the insert. (Figure 2)
Figure 1. Colonies transformed with Tenascin Fibronectin domains.
User Reviews
UNIQfb42b7a331709632-partinfo-00000000-QINU UNIQfb42b7a331709632-partinfo-00000001-QINU