Difference between revisions of "Part:BBa K3739056"
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<partinfo>BBa_K3739056 short</partinfo> | <partinfo>BBa_K3739056 short</partinfo> | ||
− | + | This is another anchored proteins onto membranes through LamB and use his tag to comformation. We use <partinfo>BBa_K3739056</partinfo> and his tag to verify LamB's function which can anchor proteins onto membranes. | |
− | + | ===Biology=== | |
− | === | + | LamB is an anchor protein from Vibrio Species, which can anchor its passenger protein to the cell membrane. It has been widely used in cell-surface display. The linker is a meaningless short peptide that we use as a control. The linker is fused with LamB used as a sandwich-anchoring motif so that the linker can be displayed on the surface of VnDX. |
+ | |||
+ | ===Characterization=== | ||
+ | ====1. Identification==== | ||
+ | After receiving the synthesized DNA, PCR was done to certify that the plasmid was correct, and the experimental results were shown in figure1. | ||
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Revision as of 05:33, 21 October 2021
J23100-B0030-LamB1-linker-LamB2-his-B0010
This is another anchored proteins onto membranes through LamB and use his tag to comformation. We use BBa_K3739056 and his tag to verify LamB's function which can anchor proteins onto membranes.
Biology
LamB is an anchor protein from Vibrio Species, which can anchor its passenger protein to the cell membrane. It has been widely used in cell-surface display. The linker is a meaningless short peptide that we use as a control. The linker is fused with LamB used as a sandwich-anchoring motif so that the linker can be displayed on the surface of VnDX.
Characterization
1. Identification
After receiving the synthesized DNA, PCR was done to certify that the plasmid was correct, and the experimental results were shown in figure1.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 676
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 824