BBa_K371043BBa_K371043 Version 1 (Component)MPF(meta-prefix)+RFP+MSF(meta-suffix)
BBa_J22000BBa_J22000 Version 1 (Component)DnaA binding sequence - Px
cln2BBa_K105014 Version 1 (Component)cln2 PEST destabilization domain for rapid protein turnover
BBa_K1461309BBa_K1461309 Version 1 (Component)pCMV-RBS-GFP-4 miR 142 5p non-bindgin sites-d.term
BBa_K1777012BBa_K1777012 Version 1 (Component)sequence-specific RNA binding protein
BBa_K1777014BBa_K1777014 Version 1 (Component)sequence-specific RNA binding protein
BBa_K1777013BBa_K1777013 Version 1 (Component)sequence-specific RNA binding protein
BBa_K1777004BBa_K1777004 Version 1 (Component)sequence-specific RNA binding protein
cssR-S2BO_2742 Version 1 (Component) BBa_K242300BBa_K242300 Version 1 (Component)multi-Ler binding site +promoter 1
BBa_K923005BBa_K923005 Version 1 (Component)Ribosome Binding Site in pET14b plasmid
BBa_K1088057BBa_K1088057 Version 1 (Component)T25 domain of bacterial two-hybrid system (IPTG inducible)
BBa_K748000BBa_K748000 Version 1 (Component)AgrA protein coding sequence. AgrA is the main component of S.aureus agr quorum sensing system.
BBa_K748001BBa_K748001 Version 1 (Component)AgrC protein coding sequence. AgrC is main component of S.aureus agr quorum sensing system.
BBa_J58008BBa_J58008 Version 1 (Component)Periplasmic binding protein that docks a vanillin molecule
GFP-AIDBBa_K812110 Version 1 (Component)GFP fusion with the ubuquitinase E3 OsTirI recoginition domain for PSC2+ plasmid
BBa_K300096BBa_K300096 Version 1 (Component)Double phasin and intein separed by a flexible protein domain linker
BBa_J64863BBa_J64863 Version 1 (Component)Strong OmpR Binding Operon for Team Challenge 03-2007
BBa_K371054BBa_K371054 Version 1 (Component)MPF(meta-prefix)+[GFP+10*GS+A] fusion protein+MSF(meta-suffix))
BBa_I758600BBa_I758600 Version 1 (Component)Screen for binding affinity of mutant cI lambda to promotor sites
BBa_I720010BBa_I720010 Version 1 (Component)Ara landing pad (pBBLP 8)
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.