Difference between revisions of "Part:BBa K1918102"
(One intermediate revision by one other user not shown) | |||
Line 3: | Line 3: | ||
<partinfo>BBa_K1918102 short</partinfo> | <partinfo>BBa_K1918102 short</partinfo> | ||
− | This part is consist of EBFP2C(155-238) and the TRE promoter. EBFP2C(155-238) is a peptied made up | + | This part is consist of EBFP2C(155-238) and the TRE promoter. EBFP2C(155-238) is a peptied made up of the 155th to 238th(C-terminus) amino acids in fluorescent protein EBFP2. TRE is the Dox induced promoter. Driven by TRE promoter, the expression of EBFP2C(155-238) could be induced by Dox. |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
Line 17: | Line 17: | ||
<partinfo>BBa_K1918102 parameters</partinfo> | <partinfo>BBa_K1918102 parameters</partinfo> | ||
<!-- --> | <!-- --> | ||
+ | |||
+ | {{Tsinghua-A}} | ||
+ | <html> | ||
+ | <div class="column full_size"> | ||
+ | <ul> | ||
+ | |||
+ | <p>In the figures are the FACS test results of our parts., which are EBFP2 without and with intein respectively. The EBFP-A signals tell us that the split florescent proteins could fuse together and emit florescent light.</p> | ||
+ | |||
+ | <div class="column full_size" > | ||
+ | <img src="https://static.igem.org/mediawiki/2016/f/fa/T--Tsinghua-A--pro0010.jpg"> | ||
+ | </div> | ||
+ | <div class="column full_size" > | ||
+ | <img src="https://static.igem.org/mediawiki/2016/4/44/T--Tsinghua-A--results0002.jpg"> | ||
+ | </div> | ||
+ | |||
+ | <p>Without Dox, constructs containing CMV show no florescent signal, which means that one single N- or C- terminal cannot light up. However, once the other half is induced, they bind and emit light.</p> | ||
+ | </ul> | ||
+ | |||
+ | |||
+ | </div> | ||
+ | |||
+ | </html> |
Latest revision as of 22:04, 19 October 2016
TRE-Kozak-EBFP2C(155-238)
This part is consist of EBFP2C(155-238) and the TRE promoter. EBFP2C(155-238) is a peptied made up of the 155th to 238th(C-terminus) amino acids in fluorescent protein EBFP2. TRE is the Dox induced promoter. Driven by TRE promoter, the expression of EBFP2C(155-238) could be induced by Dox.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 379
Illegal XbaI site found at 649 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 379
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 379
Illegal BamHI site found at 362
Illegal XhoI site found at 19 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 379
Illegal XbaI site found at 649 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 379
Illegal XbaI site found at 649 - 1000COMPATIBLE WITH RFC[1000]
In the figures are the FACS test results of our parts., which are EBFP2 without and with intein respectively. The EBFP-A signals tell us that the split florescent proteins could fuse together and emit florescent light.
Without Dox, constructs containing CMV show no florescent signal, which means that one single N- or C- terminal cannot light up. However, once the other half is induced, they bind and emit light.