Difference between revisions of "Part:BBa K4165175"
Omnia Alaa11 (Talk | contribs) |
|||
Line 5: | Line 5: | ||
This composite part consists of T7 promoter (BBa_K3633015), lac operator (BBa_K4165062), pGS-21a RBS (BBa_K4165016), 6x His-tag (BBa_K4165020), Tau (BBa_K4165009), and T7 terminator (BBa_K731721). | This composite part consists of T7 promoter (BBa_K3633015), lac operator (BBa_K4165062), pGS-21a RBS (BBa_K4165016), 6x His-tag (BBa_K4165020), Tau (BBa_K4165009), and T7 terminator (BBa_K731721). | ||
− | + | ===Source=== | |
+ | Synthesized | ||
+ | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | In the AD brain, tau Hyperphosphorylation is considered the main cause of AD progression, it may alter the protein's shape and charge, which in turn causes the microtubule-binding domain to become exposed and allow tau to self-assemble and form oligomers characterized to be a neurofibrillary tangle. According to several studies, the polymerized tau (neurofibrillary tangles) is inert since it does not bind to tubulin or encourage its assembly into microtubules, the His Tag for the purification of the protein. | ||
<!-- --> | <!-- --> | ||
===<span class='h3bb'>Sequence and Features</span>=== | ===<span class='h3bb'>Sequence and Features</span>=== | ||
<partinfo>BBa_K4165175 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4165175 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | ===Dry Lab=== | ||
+ | <p style=" font-weight: bold; font-size:14px;"> Modeling </p> | ||
+ | |||
+ | <p style=" font-weight: bold; font-size:14px;"> Mathematical modeling </p> | ||
+ | <p style=" font-weight: bold; font-size:14px;">Transcription rate and translation rate under T7 promotor </p> | ||
+ | the mathematical modeling was based on our code for the calculation of transcription and translation (you can find it in the code section) beside with the estimated results from the wet lab. | ||
+ | |||
+ | <html> | ||
+ | <p><img src="https://static.igem.wiki/teams/4165/wiki/dry-lab/mathematical-modeling/mathematical-modeling/his-tau2.png" style="margin-left:200px;" alt="" width="500" /></p> | ||
+ | </html> | ||
+ | |||
+ | |||
+ | Figure 1. this figure shows the results from the transcription and translation code showing | ||
+ | the variation of mRNA and protein concentrations with time compared with the wet lab results. | ||
Revision as of 04:26, 11 October 2022
Biobrick His - Tau
This composite part consists of T7 promoter (BBa_K3633015), lac operator (BBa_K4165062), pGS-21a RBS (BBa_K4165016), 6x His-tag (BBa_K4165020), Tau (BBa_K4165009), and T7 terminator (BBa_K731721).
Source
Synthesized
Usage and Biology
In the AD brain, tau Hyperphosphorylation is considered the main cause of AD progression, it may alter the protein's shape and charge, which in turn causes the microtubule-binding domain to become exposed and allow tau to self-assemble and form oligomers characterized to be a neurofibrillary tangle. According to several studies, the polymerized tau (neurofibrillary tangles) is inert since it does not bind to tubulin or encourage its assembly into microtubules, the His Tag for the purification of the protein.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 169
Illegal AgeI site found at 355 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 333
Illegal BsaI site found at 1245
Illegal BsaI.rc site found at 45
Illegal SapI.rc site found at 519
Dry Lab
Modeling
Mathematical modeling
Transcription rate and translation rate under T7 promotor
the mathematical modeling was based on our code for the calculation of transcription and translation (you can find it in the code section) beside with the estimated results from the wet lab.
Figure 1. this figure shows the results from the transcription and translation code showing the variation of mRNA and protein concentrations with time compared with the wet lab results.