Difference between revisions of "Team:Gifu/result-page"
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</div> | </div> | ||
<br> | <br> | ||
− | <div class="center"><b>Table.2 Ct value | + | <div class="center"><b>Table.2 Ct value at fluorescence 1.90</b><br> |
<img src="https://static.igem.org/mediawiki/2015/1/1b/Gifu-kekka-kekka.png" width="450" height="96" vspace="10" hspace="30"></img></div> | <img src="https://static.igem.org/mediawiki/2015/1/1b/Gifu-kekka-kekka.png" width="450" height="96" vspace="10" hspace="30"></img></div> | ||
<br clear="all"> | <br clear="all"> | ||
− | <p> According to this result, we calculated Ct value which indicates 1. | + | <p> According to this result, we calculated Ct value which indicates 1.90 fluorescence intensity. These value is summarized right. Ct is a value that the more the gene template in PCR increases, the more Ct value decreases. If there is a difference between “C” and “D”, there is a difference in the quantity of template geneThus, the difference between “C” and “D” is small; the cyclization may be efficiency.As a result, Ct in " |
− | + | ||
normal <a href= "http://parts.igem.org/wiki/index.php?title=Part:BBa_1332011" > [BBa_1332011]</a> | normal <a href= "http://parts.igem.org/wiki/index.php?title=Part:BBa_1332011" > [BBa_1332011]</a> | ||
" was 2.31, but “ | " was 2.31, but “ | ||
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</font> | </font> | ||
− | <br><br><br><br> | + | <br><br><br><br><blockquote><blockquote> |
<font size="4" face="Century"><b> FUNCTION </b></font> | <font size="4" face="Century"><b> FUNCTION </b></font> | ||
<font size="3"face="Arimo"> | <font size="3"face="Arimo"> | ||
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<br clear="all"> | <br clear="all"> | ||
<b>Fig.6 Overlapping Fig.4 and Fig.5 </b><br><br> | <b>Fig.6 Overlapping Fig.4 and Fig.5 </b><br><br> | ||
+ | There was not fluorescence at the place of long chain protein. We found that long chain protein didn’t have a function. | ||
+ | </br> | ||
+ | <br><br></blockquote></blockquote> | ||
<p> | <p> | ||
− | <div class="center">Table 4. The generators used to research the qualitative of a protein | + | <div class="center">Table 4. The generators used to research the qualitative of a protein</div><br> |
<table class="partsjump" align="center"> | <table class="partsjump" align="center"> | ||
<tr> | <tr> | ||
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− | < | + | <blockquote><blockquote> |
− | + | ||
− | + | ||
<br clear="all"><br> | <br clear="all"><br> | ||
− | <font size="4"face="Arimo">< | + | <font size="4"face="Arimo"><li><b>Reason of why |
<a href= "http://parts.igem.org/wiki/index.php?title=Part:BBa_K1859020" > [BBa_K1859020] </a> | <a href= "http://parts.igem.org/wiki/index.php?title=Part:BBa_K1859020" > [BBa_K1859020] </a> | ||
and | and | ||
<a href= "http://parts.igem.org/wiki/index.php?title=Part:BBa_K1859022" > [BBa_K1859022] </a> | <a href= "http://parts.igem.org/wiki/index.php?title=Part:BBa_K1859022" > [BBa_K1859022] </a> | ||
− | don’t synthesize the long chain protein</ | + | don’t synthesize the long chain protein</b></li><br> |
</font> | </font> | ||
In this experiment, | In this experiment, | ||
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We made prediction of synthesized mRNA’s secondary structure. | We made prediction of synthesized mRNA’s secondary structure. | ||
</br> | </br> | ||
+ | </blockquote></blockquote> | ||
+ | |||
<img src="https://static.igem.org/mediawiki/2015/d/d3/Gifu-%E7%92%B0%E7%8A%B62014.png" width="320" height="201" vspace="10" hspace="20" align="left"></img> | <img src="https://static.igem.org/mediawiki/2015/d/d3/Gifu-%E7%92%B0%E7%8A%B62014.png" width="320" height="201" vspace="10" hspace="20" align="left"></img> | ||
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</p> | </p> | ||
<p> | <p> | ||
+ | |||
+ | <blockquote><blockquote> | ||
We can see the mRNA which is not to synthesize a long chain protein (BBa_K1859020 and BBa_K1859022) forms hydrogen bonds in downstream of the ribosome binding site. | We can see the mRNA which is not to synthesize a long chain protein (BBa_K1859020 and BBa_K1859022) forms hydrogen bonds in downstream of the ribosome binding site. | ||
− | It is assumed that these binds prevent mRNA from starting to be translated. | + | It is assumed that these binds prevent mRNA from starting to be translated.<br><br><br> |
</p> | </p> | ||
− | + | </blockquote></blockquote> | |
Latest revision as of 20:08, 18 September 2015
normal | outside | insideⅠ | insideⅡ | |
---|---|---|---|---|
Efficiency of circularization (relativity value) | 1.00 | 2.05 | 1.22 | 1.34 |
FUNCTIONWe made 7 kinds of linker in this experiment.
We made parts which have these sequence of linker in the downstream of the 3’ side of the intron [BBa_K1332005] or the upstream of the 5’ side of the intron without stop codon [BBa_K1332003].
We constructed plasmids like following it.In case of inserting these plasmid into E. coli, the following circular mRNA is expressed and the long chain protein is synthesized.
We inserted these plasmid into an E. coli and made it synthesize proteins and did SDS-PAGE using this proteins. If the protein is not boiled, we can do SDS-PAGE keeping it fluorescence because RFP’s structure is strong. Therefore we applied samples that were not boiled.
Fig.4 Fluorescence of protein before dying by CBB Fig.5 after dying by CBB
Fig.6 Overlapping Fig.4 and Fig.5
There was not fluorescence at the place of long chain protein. We found that long chain protein didn’t have a function.
No. | generator |
---|---|
A | R0010+ B0034+ K1332001+ B0015 |
B | BBa_K1332011 |
C | BBa_K1859027 |
D | BBa_K1859028 |
E | BBa_K1859020 |
F | BBa_K1859021 |
G | BBa_K1859022 |
H | BBa_K1859023 |
I | BBa_K1859023 |
J | BBa_K1859025 |
K | BBa_K1859024 |
Reason of why [BBa_K1859020] and [BBa_K1859022] don’t synthesize the long chain protein
In this experiment, [BBa_K1859020] and [BBa_K1859022] didn’t generate the long chain protein. The reason of this phenomenon can be deduced in terms of the sequence of the circular mRNA.
We made prediction of synthesized mRNA’s secondary structure.
We can see the mRNA which is not to synthesize a long chain protein (BBa_K1859020 and BBa_K1859022) forms hydrogen bonds in downstream of the ribosome binding site. It is assumed that these binds prevent mRNA from starting to be translated.