Difference between revisions of "Part:BBa K2336026"
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[[File:oprF-LBT.jpg|400px|thumb|center|Figure1-1:oprF-LBT]] | [[File:oprF-LBT.jpg|400px|thumb|center|Figure1-1:oprF-LBT]] | ||
| − | < | + | <h2>SDS-PAGE</h2> |
| − | + | After oprF-LBT1 is expressed successfully,we centrifuged the bacteria liquid and separated different proteins by SDS-PAGE. | |
| − | + | [[File:SDS-PAGE.jpg|250px|thumb|center|Figure1-2:SDS-PAGE]] | |
| − | + | Figure shows an obvious ~31kDa protein bands of oprF-3*LBT1 in test lane, which cannot be found in control lane.This result proves that the bacteria could express oprF-LBT1 successfully. | |
| − | + | ||
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===Functional Parameters=== | ===Functional Parameters=== | ||
<partinfo>BBa_K2336026 parameters</partinfo> | <partinfo>BBa_K2336026 parameters</partinfo> | ||
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Revision as of 12:50, 30 October 2017
oprF-GS-FLAG-LBT1-GS-LBT1-GS-LBT1
The report part of our circuit. Oprf can be expressed as an anchor on the cell membrane to make sure the LBT can combine with terbium (Tb3 +) on the surface of the bacteria.
Characterization
This is a part for recycling.LBT1（lanthanide binding tag）can bind the lanthanide ions and it can be expressed at the cell membrane of E.coli with the help of oprF.We set the 'FLAG' between oprF and LBT for fluorescence detection.In our experiment,we let the LBT1 be expressed successfully which means that the lanthanide ions in the water would be bound and recycled effectively after we put the in the water.
SDS-PAGE
After oprF-LBT1 is expressed successfully,we centrifuged the bacteria liquid and separated different proteins by SDS-PAGE.
Figure shows an obvious ~31kDa protein bands of oprF-3*LBT1 in test lane, which cannot be found in control lane.This result proves that the bacteria could express oprF-LBT1 successfully.