BBa_K1362260 1 BBa_K1362260 Chitin binding domain with triglycine linker and His-tag 2014-10-08T11:00:00Z 2015-05-08T01:10:05Z false false _1738_ 0 22911 9 Not in stock false false Elisabeth Sch??fer annotation2424694 1 His-tag range2424694 1 1 18 annotation2424697 1 chitin binding domain range2424697 1 28 183 annotation2424696 1 glycine linker range2424696 1 19 27 BBa_K1362416 1 RFC105 NN* N-terminal non-splicing overhang GGCT=Gly+1/3Leu|Ile RFC[105] overhang NN* 2014-10-06T11:00:00Z 2015-05-08T01:10:05Z This standard overhang part was developed as part of the iGEM team Heidelberg 2014's Intein Toolbox [[#References|[1]]]. All standard sequences can be reviewed in RFC[???] [[#References|[2]]]. This is a standard overhang sequence for in-frame cloning of Proteins of Interest in front or behind an Intein. A detailed cloning strategy is found on the iGEM team Heidelberg 2014's [http://2014.igem.org/Team:Heidelberg/parts wiki page] as well as in RFC[???]. Specifically, this part contains the overhang B* used to insert a protein in front of a non-splicing N-Intein, which could often serve as control for protein splicing experiments. It lies within the four bases formed by the glycine and the first base of the subsequent Leucine/Isoleucine or similar of the mutated N-terminal splicing site. false false _1738_ 0 12377 9 Not in stock false This part is only the sequence of a standard overhang. It will not be sent in as physical DNA and was merely created to easily compose new parts in the RFC[???] standard. In the actual cloning process this sequence was and is recommended to be inserted with the according PCR primers. false Constantin Ahlmann-Eltze, Charlotte Bunne, Magdalena B??scher, Jan Gleixner, Max Horn, Anna Huhn, Nils Klughammer, Jakob Kreft, Elisabeth Sch??fer, Carolin Schmelas, Silvan Schmitz, Max Waldha BBa_K1362440 1 RFC105 A N-terminal start overhang (T)(A)-GATG=RBS+Start RFC[105] A 2014-10-07T11:00:00Z 2015-05-08T01:10:05Z false false _1738_ 0 22830 9 Not in stock false false Constantin Ahlmann-Eltze, Charlotte Bunne, Magdalena B??scher, Jan Gleixner, Max Horn, Anna Huhn, Nils Klughammer, Jakob Kreft, Elisabeth Sch??fer, Carolin Schmelas, Silvan Schmitz, Max Waldha BBa_K1362061 1 BBa_K1362061 N-terminal chitin binding domain with triglycine linker and His-tag as RFC[105] insert 2014-10-08T11:00:00Z 2015-05-08T01:10:04Z false false _1738_ 0 22830 9 Not in stock false false Jan Gleixner component2430374 1 BBa_K1362425 component2430380 1 BBa_K1362466 component2430379 1 BBa_K1362260 component2430382 1 BBa_K1362423 component2430375 1 BBa_K1362440 component2430381 1 BBa_K1362416 annotation2430374 1 BBa_K1362425 range2430374 1 1 6 annotation2430379 1 BBa_K1362260 range2430379 1 11 193 annotation2430380 1 BBa_K1362466 range2430380 1 194 208 annotation2430382 1 BBa_K1362423 range2430382 1 213 219 annotation2430381 1 BBa_K1362416 range2430381 1 209 212 annotation2430375 1 BBa_K1362440 range2430375 1 7 10 BBa_K1362425 1 BsaI -> BsaI restriction site for RFC[???] cloning (in part in prefix) 2014-10-07T11:00:00Z 2015-05-08T01:10:05Z This Sequence starts with a part of the BsaI recognition site. The missing G of the recognition site can be found in the upstream BB prefix. It contains a spacer nucleotide so that BsaI will cut the top strand directly downstream and the bottom strand 4 nucleotides downstream. false false _1738_ 0 22830 9 Not in stock false false Constantin Ahlmann-Eltze, Charlotte Bunne, Magdalena B&uuml;scher, Jan Gleixner, Max Horn, Anna Huhn, Nils Klughammer, Jakob Kreft, Elisabeth Sch&auml;fer, Carolin Schmelas, Silvan Schmitz, Max Waldha annotation2402282 1 RFC[???] standard overhang A range2402282 1 5 5 annotation2400588 1 BsaI site range2400588 1 1 5 BBa_K1362423 1 <- BsaI BsaI reverse restriction site for RFC[105] cloning 2014-10-06T11:00:00Z 2015-05-08T01:10:05Z This standard restriction site sequence is used as part of the iGEM team Heidelberg 2014's Intein Toolbox [[#References|[1]]]. All associated standard sequences can be reviewed in RFC[???] This is the reverse complement of a BsaI restriction site headed by an Adenine as a spacer-base to separate the recognition sequence from the outward-lying cutting sequence. It was used by us for scarless golden-gate cloning to fuse inteins to other proteins and thereby implement a variety of possible port-translational modifications. false false _1738_ 0 12377 9 Not in stock false This part is only the sequence of a restriction site. It will not be sent in as physical DNA and was merely created to easily compose new parts in the RFC[???] standard. In the actual cloning process this sequence was and is recommended to be inserted with the according PCR primers. false Constantin Ahlmann-Eltze, Charlotte Bunne, Magdalena B??scher, Jan Gleixner, Max Horn, Anna Huhn, Nils Klughammer, Jakob Kreft, Elisabeth Sch??fer, Carolin Schmelas, Silvan Schmitz, Max Waldha BBa_K1362466 1 BBa_K1362466 Intein protease extein 2014-10-08T11:00:00Z 2015-05-08T01:10:06Z false false _1738_ 0 22830 9 Not in stock false false Jan Gleixner BBa_K1362425_sequence 1 gtctcc BBa_K1362466_sequence 1 ctgcgtgaatctggt BBa_K1362423_sequence 1 agagacc BBa_K1362440_sequence 1 gatg BBa_K1362061_sequence 1 gtctccgatgcatcatcaccatcaccacggtggaggtaccacaaatcctggtgtatccgcttggcaggtcaacacagcttatactgcgggacaattggtcacatataacggcaagacgtataaatgtttgcagccccacacctccttggcaggatgggaaccatccaacgttcctgccttgtggcagcttcaactgcgtgaatctggtggctagagacc BBa_K1362260_sequence 1 catcatcaccatcaccacggtggaggtaccacaaatcctggtgtatccgcttggcaggtcaacacagcttatactgcgggacaattggtcacatataacggcaagacgtataaatgtttgcagccccacacctccttggcaggatgggaaccatccaacgttcctgccttgtggcagcttcaa BBa_K1362416_sequence 1 ggct igem2sbol 1 iGEM to SBOL conversion Conversion of the iGEM parts registry to SBOL2.1 James Alastair McLaughlin Chris J. Myers 2017-03-06T15:00:00.000Z