Difference between revisions of "Part:BBa K5332000:Experience"
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Transfection of the plasmid into E. coli EcN synthetic engineering bacterium FMK and gavage to mice with intestinal inflammation, it can be found that the shortening of the length of the mouse colon is restored, the recruitment of immune cells is inhibited, the intestinal beneficial bacteria are enriched, the diversity of the intestinal flora is increased, and the up-regulation of pro-inflammatory factors and anti-inflammatory factors down-regulation are inhibited accordingly. The above results indicate that the gene elements designed by our team can fully exert the expected effect in the vector cell EcN with good results. | Transfection of the plasmid into E. coli EcN synthetic engineering bacterium FMK and gavage to mice with intestinal inflammation, it can be found that the shortening of the length of the mouse colon is restored, the recruitment of immune cells is inhibited, the intestinal beneficial bacteria are enriched, the diversity of the intestinal flora is increased, and the up-regulation of pro-inflammatory factors and anti-inflammatory factors down-regulation are inhibited accordingly. The above results indicate that the gene elements designed by our team can fully exert the expected effect in the vector cell EcN with good results. | ||
| − | Our elements can be used for spatiotemporal specificity to exert a mitigating effect on inflammation where the level of inflammation is high in the intestinal tract. | + | <partinfo>Our elements can be used for spatiotemporal specificity to exert a mitigating effect on inflammation where the level of inflammation is high in the intestinal tract.</partinfo> |
===User Reviews=== | ===User Reviews=== | ||
Revision as of 06:33, 2 October 2024
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_K5332000
Transfection of the plasmid into E. coli EcN synthetic engineering bacterium FMK and gavage to mice with intestinal inflammation, it can be found that the shortening of the length of the mouse colon is restored, the recruitment of immune cells is inhibited, the intestinal beneficial bacteria are enriched, the diversity of the intestinal flora is increased, and the up-regulation of pro-inflammatory factors and anti-inflammatory factors down-regulation are inhibited accordingly. The above results indicate that the gene elements designed by our team can fully exert the expected effect in the vector cell EcN with good results.
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User Reviews
UNIQ701afdcab66815b8-partinfo-00000001-QINU UNIQ701afdcab66815b8-partinfo-00000002-QINU