Difference between revisions of "Part:BBa K4497011"
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<partinfo>BBa_K4497011 short</partinfo> | <partinfo>BBa_K4497011 short</partinfo> | ||
− | + | This part encodes the intracellular protease function of the MESA system. We used it in combination with mCherry and GFP nanobodies (see [[Part:Bba_K4497017]]). | |
+ | |||
+ | ==Design & Cloning== | ||
+ | ===Design=== | ||
+ | This part is made of the following components: | ||
+ | |||
+ | * CD 28 transmembrane domain ([[Part:BBa_K4497004]]): transmembrane anchor for the MESA system | ||
+ | * Tobacco Etch Virus (TEV) Protease ([[Part:BBa_K4497005]]): Protease cleaving proteins the TEV recognition site | ||
+ | |||
+ | ===Cloning=== | ||
+ | *G1TA: [[Part:BBa_K4497017]] | ||
+ | *G1TEV: [[Part:BBa_K4497018]] | ||
+ | *M1TA: [[Part:BBa_K4497019]] | ||
+ | *M1TEV: [[Part:BBa_K4497020]] | ||
+ | *G2TA: [[Part:BBa_K4497021]] | ||
+ | *G2TEV: [[Part:BBa_K4497022]] | ||
+ | *M2TA: [[Part:BBa_K4497023]] | ||
+ | *M2TEV: [[Part:BBa_K4497024]] | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 14:07, 13 October 2022
TEV MESA Part
This part encodes the intracellular protease function of the MESA system. We used it in combination with mCherry and GFP nanobodies (see Part:Bba_K4497017).
Design & Cloning
Design
This part is made of the following components:
- CD 28 transmembrane domain (Part:BBa_K4497004): transmembrane anchor for the MESA system
- Tobacco Etch Virus (TEV) Protease (Part:BBa_K4497005): Protease cleaving proteins the TEV recognition site
Cloning
- G1TA: Part:BBa_K4497017
- G1TEV: Part:BBa_K4497018
- M1TA: Part:BBa_K4497019
- M1TEV: Part:BBa_K4497020
- G2TA: Part:BBa_K4497021
- G2TEV: Part:BBa_K4497022
- M2TA: Part:BBa_K4497023
- M2TEV: Part:BBa_K4497024
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 448
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 448
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 448
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 448
- 1000COMPATIBLE WITH RFC[1000]