Difference between revisions of "Part:BBa K4202025:Experience"
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===Applications of BBa_K4202025=== | ===Applications of BBa_K4202025=== | ||
+ | <br> | ||
+ | ==Characterization== | ||
+ | <b>Vector construct</b> | ||
+ | To characterization this part, we constructed the measurement device <partinfo>BBa_K4202033</partinfo> and then constructed it to the pHY300PLK plasmid. The vector was then transformed into <i>Bacillus subtilis</i> WB600 strain. | ||
+ | <br> | ||
+ | </p>The transformant were inoculate to 2ml LB medium and cultured in the test tube overnight. The next day, the culture were inoculated into 2ml TB medium containing 0%, 0.1%, 0.5%, 1%, 2%, 5% sucrose (w/v) at the ratio of 1:100. After cultured in 37℃, 220rpm for 7 hours, the culture were diluted into PBS at the ratio of 1:1000 and were measured the fluorescence intensity through flow cytometry.</p> | ||
+ | <br> | ||
===User Reviews=== | ===User Reviews=== |
Revision as of 14:13, 12 October 2022
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_K4202025
Characterization
Vector construct
To characterization this part, we constructed the measurement device BBa_K4202033 and then constructed it to the pHY300PLK plasmid. The vector was then transformed into Bacillus subtilis WB600 strain.
</p>The transformant were inoculate to 2ml LB medium and cultured in the test tube overnight. The next day, the culture were inoculated into 2ml TB medium containing 0%, 0.1%, 0.5%, 1%, 2%, 5% sucrose (w/v) at the ratio of 1:100. After cultured in 37℃, 220rpm for 7 hours, the culture were diluted into PBS at the ratio of 1:1000 and were measured the fluorescence intensity through flow cytometry.</p>
User Reviews
UNIQea9cedb324584182-partinfo-00000001-QINU UNIQea9cedb324584182-partinfo-00000002-QINU