Difference between revisions of "Team:Brasil-USP/Parts/Listofparts"
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+ | |||
+ | <center> | ||
+ | <table style="width:95%" border="5" bordercolor="white"> | ||
+ | <tr bgcolor="#D8D8D8"> | ||
+ | <td width=13%><b><center>Registry Code</b></center></td> | ||
+ | <td width=14%><b><center>Name</b></center></td> | ||
+ | <td width=13%><b><center>Role</b></center></td> | ||
+ | <td width=53%><b><center>Description</center></b></td> | ||
+ | <td width=7%><b><center>Length (bp)</center></b></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#04A872" height="100"> | ||
+ | <td><center>BBa_K1819003</center></td> | ||
+ | <td><center>RoxA</center></td> | ||
+ | <td><center>Protein coding</center></td> | ||
+ | <td><center>Rubber oxygenase A (Rox A) from <i>Xanthomonas sp.</i> strain 35Y- catalyzes oxidative C-C cleavage of | ||
+ | poly(cis-1,4-isoprene)</center></td> | ||
+ | <td><center>1954</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#04A872" height="100"> | ||
+ | <td><center>BBa_K1819001</center></td> | ||
+ | <td><center>Lcp</center></td> | ||
+ | <td><center>Role</center></td> | ||
+ | <td><center>Latex clearing protein (Lcp) from <i>Streptomyces sp.</i> strain K30 | ||
+ | - catalyzes rubber cleavage at the | ||
+ | cis double bonds</center></td> | ||
+ | <td><center>1138</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#04A872" height="80"> | ||
+ | <td><center>BBa_K1819000</center></td> | ||
+ | <td><center>Linker-GFP</center></td> | ||
+ | <td><center>Reporter part</center></td> | ||
+ | <td><center>It is a GFP coding sequence with an N-terminal linker, which is 5’-flanked by NdeI restriction site</center></td> | ||
+ | <td><center>750</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#04A872" height="80"> | ||
+ | <td><center>BBa_K1819002</center></td> | ||
+ | <td><center>TAT signal</center></td> | ||
+ | <td><center>Signalling part</center></td> | ||
+ | <td><center>Twin-arginine translocation signal</center></td> | ||
+ | <td><center>147</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="80"> | ||
+ | <td><center>BBa_K1819004</center></td> | ||
+ | <td><center>GFP_I13507</center></td> | ||
+ | <td><center>Composite part</center></td> | ||
+ | <td><center>RFP regulation through promoter tetR (part R0040), dependent of tetracycline</center></td> | ||
+ | <td><center>2499</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="100"> | ||
+ | <td><center>BBa_K1819005</center></td> | ||
+ | <td><center>J23101 + linkerGFPTerm</center></td> | ||
+ | <td><center>Characterization circuit</center></td> | ||
+ | <td><center>Constitutive promotor from Anderson library (BBa_J23101) assembled to green fluorescent protein attached to linker</center></td> | ||
+ | <td><center>930</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="100"> | ||
+ | <td><center>BBa_K1819006</center></td> | ||
+ | <td><center>J23106 + linkerGFPTerm</center></td> | ||
+ | <td><center>Characterization circuit</center></td> | ||
+ | <td><center>Constitutive promoter from Anderson library (BBa_J23106) assembled to green fluorescent protein attached to linker</center></td> | ||
+ | <td><center>930</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="100"> | ||
+ | <td><center>BBa_K1819007</center></td> | ||
+ | <td><center>J23117 + linkerGFPTerm</center></td> | ||
+ | <td><center>Characterization circuit</center></td> | ||
+ | <td><center>Constitutive promotor from Anderson library (BBa_J23117) assembled to green fluorescent protein attached to linker</center></td> | ||
+ | <td><center>930</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="80"> | ||
+ | <td><center>BBa_K1819008</center></td> | ||
+ | <td><center>Pl_I13507</center></td> | ||
+ | <td><center>Construction promoter test</center></td> | ||
+ | <td><center>Promoter test circuit to analyze the kill switch efficiency</center></td> | ||
+ | <td><center>2725</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="80"> | ||
+ | <td><center>BBa_K1819009</center></td> | ||
+ | <td><center>pVeg + GFP_Term</center></td> | ||
+ | <td><center>Characterization circuit</center></td> | ||
+ | <td><center>This device express GFP under a strong constitutive Bacillus promoter control (pVeg) (BBa_K823003)</center></td> | ||
+ | <td><center>1123</center></td> | ||
+ | |||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="80"> | ||
+ | <td><center>BBa_S05291</center></td> | ||
+ | <td><center>RBS-OmpA</center></td> | ||
+ | <td><center>Construction intermediate</center></td> | ||
+ | <td><center>It is composed of a RBS preceding an outer membrane protein A (OmpA), that displays proteins on cell surface.</center></td> | ||
+ | <td><center>484</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="100"> | ||
+ | <td><center>BBa_S05307</center></td> | ||
+ | <td><center>GFP_P0440</center></td> | ||
+ | <td><center>Construction intermediate</center></td> | ||
+ | <td><center>This construction gives the possibility of adding the most suitable promoter in order to regulate GFP transcription and any genetic sequence inserted after RBS and before TetR</center></td> | ||
+ | <td><center>1568</center></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr bgcolor="#D8D8D8" height="80"> | ||
+ | <td><center>BBa_S05308</center></td> | ||
+ | <td><center>Linker-GFP_Term</center></td> | ||
+ | <td><center>Construction intermediate</center></td> | ||
+ | <td><center>It is an intermediate construction of the export test circuit fused to a terminal region</center></td> | ||
+ | <td><center>887</center></td> | ||
+ | </tr> | ||
+ | |||
+ | |||
+ | </table></center> | ||
</div> | </div> | ||
+ | |||
+ | <hr class="fancy-line" /> | ||
</html> | </html> | ||
+ | |||
+ | {{:Team:Brasil-USP/Templates/Foot}} |
Latest revision as of 20:46, 18 September 2015
List of Parts