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- ...to secrete small peptides using the <i>E. coli</i> microcin V (MccV) type I secretion system (T1SS) shown in Figure 2 of our <html><a href="https://202 ...type. Type 3p and 3q parts assemble as if they were a single Type 3 part.</i> </center>10 KB (1,570 words) - 11:06, 12 October 2023
- combination with tetR-mScarlet-I as the acceptor (<a ...Figure 1: How our Part Collection can be Used to Engineer New Staples</b></i>29 KB (3,930 words) - 12:30, 2 October 2024
- ...4.1"><span class="tocnumber">4.1</span> <span class="toctext"><i>In vitro</i> DNA binding</span></a></li> ...#4.2"><span class="tocnumber">4.2</span> <span class="toctext"><i>In vivo</i> DNA binding</span></a></li>30 KB (4,227 words) - 11:55, 2 October 2024
- ...to secrete small peptides using the <i>E. coli</i> microcin V (MccV) type I secretion system (T1SS) shown in Figure 2 of our <html><a href="https://202 ...type. Type 3p and 3q parts assemble as if they were a single Type 3 part.</i> </center>9 KB (1,478 words) - 11:06, 12 October 2023
- ...YNB (Yeast Nitrogen Base)). To induce the GTH1 promoter, we added 0.005% (i.e., 0.05 g/L) glucose and incubated the cultures at 28°C for 48 hours to p ..., YASARA with the FoldX plugin, and PyMOL were utilized as modeling tools. I-TASSER predicts the 3D coordinates of protein models based on sequence-to-s46 KB (6,635 words) - 06:01, 1 October 2024
- ...to secrete small peptides using the <i>E. coli</i> microcin V (MccV) type I secretion system (T1SS) shown in Figure 2 of our <html><a href="https://202 ...type. Type 3p and 3q parts assemble as if they were a single Type 3 part.</i> </center>9 KB (1,417 words) - 09:38, 12 October 2023
- ...="#5"><span class="tocnumber">5</span> <span class="toctext"><i>In Silico</i> Characterization using DaVinci</span></a> ...n class="toctext">Enhancer Hijacking is Successfully Studied <i>In Silico</i></span></a>71 KB (8,857 words) - 13:23, 2 October 2024
- ...to secrete small peptides using the <i>E. coli</i> microcin V (MccV) type I secretion system (T1SS) shown in Figure 2 of our <html><a href="https://202 ...type. Type 3p and 3q parts assemble as if they were a single Type 3 part.</i> </center>15 KB (2,296 words) - 11:32, 12 October 2023
- * '''(I, J)''' Progression of shoot growth and root induction. Kim M, Kim SC, Song KJ, Kim HB, Kim IJ, Song EY, Chun SJ (2010) Transformation of carotenoid biosynthetic genes35 KB (4,884 words) - 13:25, 2 October 2024
- ...: Example how the part collection can be used to engineer new staples</b></i> ...ing of new staples, ensuring functionality <i>in vitro</i> and <i>in vivo</i>. We took special care to include43 KB (6,020 words) - 15:19, 30 September 2024
- ...onstrated efficient cleavage of the GFLG linker by cathepsin B <i>in vivo</i> when cells were Peptide Linker GFLG Is Cleaved by Cathepsin B <i>in Vivo</i></a>46 KB (6,095 words) - 12:34, 2 October 2024
- class="toctext"><i>In Silico</i> Characterization using DaVinci</span></a> is Successfully Studied <i>In Silico</i></span></a>51 KB (5,576 words) - 13:05, 2 October 2024
- ...a_K5117000)</a></html> and the <i>bglA</i> gene of <i>Bacillus halodurans</i> <html><a href=„https://parts.igem.org/Part:BBa_K5117007">(BBa_K5117007)< <b>Target organism:</b> <i>Bacillus subtilis</i>42 KB (6,444 words) - 13:15, 2 October 2024
- ...rtho-ring cleavage of catechol, a phenolic compound (Cao ''et al''., 2008, Kim ''et al''., 2006). Since catechol is the intermediate of various metabolism Optimal pH: 7.5~8 (Kim ''et al''., 2006).18 KB (2,705 words) - 18:50, 18 September 2015
- <h1>Cathepsin B-Cleavable <i>Trans</i>-Activator: NLS-Gal4-GFLG-VP64</h1> <p>This composite part encodes a cathepsin B-cleavable <i>trans</i>-activator fusion protein. It is composed of an42 KB (5,642 words) - 12:28, 2 October 2024
- cathepsin B <i>in vivo</i>. Furthermore, we showed that wild-type cathepsin B matured into its active ...Figure 1: How our part collection can be used to engineer new staples</b></i>35 KB (4,676 words) - 12:32, 2 October 2024
- ...ing enzyme immobilisation or purification using silica-based spin columns (Kim et al., 2020). ...hind each letter represented different colonies from Blue-White Screening. I: C-terminal L2NC-tagged Tri-PETase. The ladder used: 1 kb DNA Ladder from N11 KB (1,645 words) - 13:47, 12 October 2022
- ...17000)</a></html> and the <i>bglA</i> gene of <i>Acetivibrio thermocellus</i> <html><a href="https://parts.igem.org/Part:BBa_K5117009">(BBa_K5117009)</a <b>Target organism:</b> <i>Bacillus subtilis</i>32 KB (4,773 words) - 08:33, 2 October 2024
- ...5117000)</a></html> and the <i>bglB</i> gene of <i>Paenibacillus polymyxa</i> <html><a href="https://parts.igem.org/Part:BBa_K5117008">(BBa_K5117008)</a <b>Target organism:</b> <i>Bacillus subtilis</i>33 KB (4,992 words) - 08:34, 2 October 2024
- ...BBa_K5117000)</a></html> and the <i>eglS</i> gene of <i>Bacillus subtilis</i> <html><a href="https://parts.igem.org/Part:BBa_K5117001">(BBa_K5117001)</a <b>Target organism:</b> <i>Bacillus subtilis</i>26 KB (3,973 words) - 20:41, 2 December 2024