BBa_K176175BBa_K176175 Version 1 (Component)aTc&AHL->PoPS: pCon 0.70->tetR-LVA+pCon 0.04->luxR+pLux/Tet->PoPS
BBa_K176135BBa_K176135 Version 1 (Component)aTc&AHL->PoPS: pCon 0.70->tetR-LVA+pCon 0.36->luxR+pLux/Tet->PoPS
BBa_K896599BBa_K896599 Version 1 (Component)Strophurus rankini voucher AMS R140490 NADH dehydrogenase subunit 4 (ND4) gene, partial cds; tRNA-Hi
BBa_K137037BBa_K137037 Version 1 (Component)Device with GFP with (A)24 repeat after start codon
BBa_K1766008BBa_K1766008 Version 1 (Component)EnvZ_V5 osmoregulatory histidine kinase from <i>E.coli</i>.
BBa_K1766014BBa_K1766014 Version 1 (Component)EnvZ osmoregulatory histidine kinase from <i>E.coli.</i>
BBa_K2088006BBa_K2088006 Version 1 (Component)It encodes a kind of protein named 2Fe-2S ferredoxin, a 2Fe-2S iron-sulfur cluster binding domain. I
luxR-ndhBBa_K1036000 Version 1 (Component)lux pL controlled luxR with lux pR controlled ndh (LVA-tag) coding for NADH dehydrogenase II
BBa_K749010BBa_K749010 Version 1 (Component)Formate dehydrogenase device
BBa_K749013BBa_K749013 Version 1 (Component)Formate dehydrogenase device
BBa_K1676120BBa_K1676120 Version 1 (Component)Mutant 16 of Lactate Dehydrogenase
BBa_K1676114BBa_K1676114 Version 1 (Component)Mutant 10 of Lactate Dehydrogenase
BBa_K809603BBa_K809603 Version 1 (Component)Bovine Pancreatic DNase I (in yeast mt codon table)
CAD1en2BBa_K1658001 Version 1 (Component)Cinnamyl alcohol dehydrogenase CAD1 - 2
BBa_J107021BBa_J107021 Version 1 (Component)aTc sensor (J23106 promoter) with GFP
SEGASEGA_collection Version 1 (Collection)In the Standardized Genome Architecture (SEGA), genomic integration of DNA fragments is enabled by λ-Red recombineering and so-called landing pads that are a common concept in synthetic biology and typically contain features that i) enable insertion of additional genetic elements and ii) provide well-characterized functional parts such as promoters and genes, and iii) provides insulation against genome context-dependent effects. The SEGA landing pads allow for reusable homology regions and time-efficient construction of parallel genetic designs with a minimal number of reagents and handling steps. SEGA bricks, typically synthetic DNA or PCR fragments, are integrated on the genome simply by combining the two reagents (i.e. competent cells and DNA), followed by incubation steps, and successful recombinants are identified by visual inspection on agar plates. The design of the SEGA standard was heavily influenced by the Standard European Vector Architecture (SEVA). SEGA landing pads typically hosts two major genetic “control elements” that influence gene expression on the transcriptional (C1), and translational (C2) level. Furthermore, landing pads contain gadgets such as selection and counterselection markers.