BBa_K1541000
BBa_K1541000 Version 1 (Component)
promoter lux pR with riboregulator RR12y

BBa_K1654006
BBa_K1654006 Version 1 (Component)
LuxR (vibrio harveyi) induced expression of Alyteserin-1a

BBa_K327015
BBa_K327015 Version 1 (Component)
Lux activated, C1lam repressed switch

BBa_K1106010
BBa_K1106010 Version 1 (Component)
LuxI generator with strong RBS and double terminator

BBa_J10065
BBa_J10065 Version 1 (Component)
LuxI from V. fischeri C0061 with LVA tag removed

BBa_J10064
BBa_J10064 Version 1 (Component)
Lux Operon Vibrio fischeri from part K325909

BBa_K1073017
BBa_K1073017 Version 1 (Component)
Lux I + LVA with RBS and double terminator

BBa_K145274
BBa_K145274 Version 1 (Component)
LuxI generator controlled by a AND-gate system.

BBa_K1718005
BBa_K1718005 Version 1 (Component)
LuxI and GFP behind a Bxb1 compatible genetic switch

BBa_K395102
BBa_K395102 Version 1 (Component)
GFP reporter repressed by LuxR and 3OC6HSL (K395005:K121013)

BBa_K395103
BBa_K395103 Version 1 (Component)
GFP reporter repressed by LuxR and 3OC6HSL (K395006:K121013)

BBa_K290001
BBa_K290001 Version 1 (Component)
constitutive RhlR with bicistronic LuxI - GFP controlled by pRhl

BBa_K1541025
BBa_K1541025 Version 1 (Component)
sfGFP under promoter P(Lux) with riboregulator RR12y

BBa_K132016
BBa_K132016 Version 1 (Component)
luxI+KanR-LVA+LacI+PL+KanR-LVA+aiiA+terminator

BBa_J329001
BBa_J329001 Version 1 (Component)
Simple lux-based QS circuit expressing untagged GFP

BBa_K1073008
BBa_K1073008 Version 1 (Component)
Lux I synthetase + LVA with subsequent double terminator

BBa_K415005
BBa_K415005 Version 1 (Component)
pLux/cI-OR : RBS-mCherry : Term : p(tetR) : RBS-luxR : Term

BBa_I13211
BBa_I13211 Version 1 (Component)
Biobricked version of the natural Lux quorum sensing system

BBa_K180005
BBa_K180005 Version 1 (Component)
GoL - Primary plasmid (part 1)/RPS - Paper primary plasmid (part 1) [LuxR generator]

SEGA
SEGA_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.