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- ...e mutations F160A & F126A deplete its binding capacity <html><a href="#1">[1]</a></html> . ...ernative exons by binding to “UGCAUG” RNA sequence <html><a href="#1">[1]</a></html>. Orthologs are present in a wide range of multicellular eukarya11 KB (1,743 words) - 02:56, 28 October 2020
- ...e mutations F160A & F126A deplete its binding capacity <html><a href="#1">[1]</a></html> . ...ernative exons by binding to “UGCAUG” RNA sequence <html><a href="#1">[1]</a></html>. Orthologs are present in a wide range of multicellular eukarya11 KB (1,726 words) - 02:55, 28 October 2020
- ...which participate in biodegradation of polycyclic aromatic hydrocarbons. [1–3] This part encodes for the same protein as <html><a href="https://parts ...as an electron transport chain, facilitating electron transfer from NADH [1].This system is crucial for supplying electrons to various dioxygenase syst29 KB (4,203 words) - 09:22, 2 October 2024
- ...represents a valuable and versatile set of BioBricks. Here we describe Fox-1 RBD, a protein domain able to recognise and bind a specific RNA sequence. ...ernative exons by binding to “UGCAUG” RNA sequence <html><a href="#1">[1]</a></html>. Orthologs are present in a wide range of multicellular eukarya11 KB (1,710 words) - 03:01, 28 October 2020
- ...represents a valuable and versatile set of BioBricks. Here we describe Fox-1 RBD, a protein domain able to recognise and bind a specific RNA sequence. ...ernative exons by binding to “UGCAUG” RNA sequence <html><a href="#1">[1]</a></html>. Orthologs are present in a wide range of multicellular eukarya11 KB (1,730 words) - 02:55, 28 October 2020
- ...e gene circuit of Snakin-1 peptide is consist of CamV 35s promoter, snakin-1 gene, 6xHis affinity tag, NOS terminator. <center><b>Figure 1. The expression of Snakin-1 by engineered Trichoderma atroviride</b></center>10 KB (1,515 words) - 15:29, 11 October 2022
- ...eate the new part BBa_K3605010. The identification result is showed in Fig.1. [[File:K3605010-1.jpg|center]]85 KB (13,199 words) - 14:09, 11 October 2023
- {|border="1" ...ctive in driving gene expression in E. coli, the relative expression level may vary depending on the gene fused to the promoter and on the E. coli strain62 KB (9,625 words) - 06:39, 2 October 2024
- ...udies, a hypothetical model of action of Snakin-1 was proposed that Snakin-1 affects the fungus by triggering apoptosis via multiple pathways. It also p <center><b>Figure 1. The expression of Snakin-1 by engineered Trichoderma atroviride</b></center>10 KB (1,496 words) - 15:58, 11 October 2022
- ...induced expression. Despite gel confirming a rather large, approximately 2.1 kb insert band, our sequencing results with the VR primer and BamHI RFP rev Fig 1 indicates that pPepT induces the expression of the downstream gene mRFP wit66 KB (8,421 words) - 06:22, 12 October 2022
- ...ompetent plasmid. We selected 583bp specific fragment of AtCRE1 gene (Lane 1 ) and the whole length of PTP2+GFP (Lane 4) to test transformation. Then we ...e 1. Gel electrophoresis results of P16 genome amplifying AtCRE1 gene(Lane 1), transformed strain genome amplifying AtCRE1(Lane 2), P16 genome amplifyin68 KB (9,044 words) - 15:12, 11 October 2023
- ...cription buffer, ARK-shRNA-1 can be generated within 30 minutes. ARK-shRNA-1 is designed to silence Phyllotreta striolata Aldose reductase gene, the tar ==1. Usage==10 KB (1,473 words) - 11:38, 16 October 2018
- ...or ARK-shRNA-1 generation through in vitro transcription system. ARK-shRNA-1 is designed to silence Phyllotreta striolata Arginine Kinase gene, the targ ==1. Usage==10 KB (1,437 words) - 14:18, 15 October 2018
- ...derived from the trp and lac promoters, that are regulated by trp and lac [1]. This part also exist together with lacI, part [[Part:BBa_K180000|BBa_K180 [1] Proc. Natl. Acad. Sci. USA, Vol. 80, pp. 21-2527 KB (4,267 words) - 13:39, 1 October 2024
- ...or GLS-shRNA-1 generation through in vitro transcription system. GLS-shRNA-1 is designed to silence Phyllotreta striolata Glutathione S-transferase gene ==1. Usage==10 KB (1,436 words) - 14:35, 15 October 2018
- ...points[j][0] - 1.5)*tick_diff - Math.floor((acc_exposed_datapoints[j][0] - 1)/200)*200*tick_diff).toFixed(0)).toString() + 'px\'></div>');}}}catch(err){ ...points[j][0] - 1.5)*tick_diff - Math.floor((acc_exposed_datapoints[j][0] - 1)/200)*200*tick_diff).toFixed(0)).toString() + 'px\'></div>');}}}catch(err){73 KB (7,853 words) - 16:07, 31 October 2017
- .../Materials#Autoinduction_medium autoinduction] and manual induction with 0,1 % rhamnose) and cultivation time (6 to 24 h). Furthermore it was * antibiotics: 60 µg mL<sup>-1</sup> chloramphenicol57 KB (8,638 words) - 03:38, 30 September 2024
- ...cription buffer, ARK-shRNA-1 can be generated within 30 minutes. GLS-shRNA-1 is designed to silence Phyllotreta striolata Glutathione S-transferase gene ==1. Usage==10 KB (1,495 words) - 11:38, 16 October 2018
- ...n antibody capturing and neutralizing enzymes of the β-lactamase B class [1]. <br> As CDR acceptor (also called "scaffold") we used the nanobody cAbBCII-10 [1] (or also NbBcII10 [2] or 3DWT [3], from here on called "3DWT"). This Nanob56 KB (8,191 words) - 03:28, 28 October 2020
- ...in which the sequence provided in the part would first have to be mutated [1]. ...e 1: Map of the used nanobody scaffold 3DWT. Marked in purple are the CDRs 1 to 3 and in grey the framework regions. This map was generated with SnapGen57 KB (8,247 words) - 03:32, 28 October 2020