Difference between revisions of "Part:BBa K2719005:Experience"
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===Applications of BBa_K2719005=== | ===Applications of BBa_K2719005=== | ||
| − | This part was cloned on pSB1C3 using EcoRI and PstI, later it was transformed on E.coli DH5a (Figure 1). | + | <p>This part was cloned on pSB1C3 using EcoRI and PstI, later it was transformed on <i>E.coli</i> DH5a (Figure 1).</p> |
| + | [[file:T--TecCEM--BBTCD5Colonies.png|500px]] | ||
| + | <p><i>Figure 1.</i> Colonies transformed with the Tenascin 5 Domain V Expression device</p> | ||
| − | Then the plasmid was extracted and run on an agarose gel electrophoresis (Figure 2). Later an restriction was performed using NotI and was run on an agarose gel (Figure 3) to probe the presence of the insert. Later the extracted plasmid was transformed on E.coli BL21 (DE3). | + | <p>Then the plasmid was extracted and run on an agarose gel electrophoresis (Figure 2). Later an restriction was performed using NotI and was run on an agarose gel (Figure 3) to probe the presence of the insert. Later the extracted plasmid was transformed on <i>E.coli</i> BL21 (DE3).</p> |
| − | The E.coli BL21 (DE3) colonies were later inoculated on liquid media (seed culture) and incubated overnight. From the seed culture 1 ml was inoculated on fresh LB+CAM broth, and at regular intervals the absorbance was measured. When the absorbance reached 0.7, IPTG was added to a final concentration of 1 mM and samples were taken after 5 and 16 h. Those samples were lysed. The lysate was loaded into a 18% polyacrylamide SDS-PAGE (Figure 4), from which a higher presence of protein was detected at 5 h after induction. | + | <p>The <i>E.coli</i> BL21 (DE3) colonies were later inoculated on liquid media (seed culture) and incubated overnight. From the seed culture 1 ml was inoculated on fresh LB+CAM broth, and at regular intervals the absorbance was measured. When the absorbance reached 0.7, IPTG was added to a final concentration of 1 mM and samples were taken after 5 and 16 h. Those samples were lysed. The lysate was loaded into a 18% polyacrylamide SDS-PAGE (Figure 4), from which a higher presence of protein was detected at 5 h after induction.</p> |
===User Reviews=== | ===User Reviews=== | ||
Revision as of 16:58, 17 October 2018
This experience page is provided so that any user may enter their experience using this part.
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how you used this part and how it worked out.
Applications of BBa_K2719005
This part was cloned on pSB1C3 using EcoRI and PstI, later it was transformed on E.coli DH5a (Figure 1).
Figure 1. Colonies transformed with the Tenascin 5 Domain V Expression device
Then the plasmid was extracted and run on an agarose gel electrophoresis (Figure 2). Later an restriction was performed using NotI and was run on an agarose gel (Figure 3) to probe the presence of the insert. Later the extracted plasmid was transformed on E.coli BL21 (DE3).
The E.coli BL21 (DE3) colonies were later inoculated on liquid media (seed culture) and incubated overnight. From the seed culture 1 ml was inoculated on fresh LB+CAM broth, and at regular intervals the absorbance was measured. When the absorbance reached 0.7, IPTG was added to a final concentration of 1 mM and samples were taken after 5 and 16 h. Those samples were lysed. The lysate was loaded into a 18% polyacrylamide SDS-PAGE (Figure 4), from which a higher presence of protein was detected at 5 h after induction.
User Reviews
UNIQc8206b2a0b163f9d-partinfo-00000000-QINU UNIQc8206b2a0b163f9d-partinfo-00000001-QINU