BBa_K145104
BBa_K145104 Version 1 (Component)
T7 PoPS + RiboLock -> LacI -> inhibition of LuxI

BBa_K204022
BBa_K204022 Version 1 (Component)
3O₆HSL generater device

BBa_K1616003
BBa_K1616003 Version 1 (Component)
VVD link to YC155 (YFP Cter split)

BBa_K1616004
BBa_K1616004 Version 1 (Component)
VVD linked to YN155 (YFP Nter split)

BBa_K327003
BBa_K327003 Version 1 (Component)
pBad controlled lux membrane protein

BBa_I12026
BBa_I12026 Version 1 (Component)
Test of BBa_R0011 (LacI regulated) using YFP

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

BBa_I15024
BBa_I15024 Version 1 (Component)
Tet-repressible polycistronic CFP/YFP under B0034

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

BBa_I718001
BBa_I718001 Version 1 (Component)
ech My new test generator part Feruloyl CoA hydratase for vanilin

BBa_K1352003
BBa_K1352003 Version 1 (Component)
Ice Nucleation Protein with YFP and His-tag

BBa_J70459
BBa_J70459 Version 1 (Component)
yfp RBS, {0,5;15,10} family member - B0031 simulator (reverse oligo)

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_K1718005
BBa_K1718005 Version 1 (Component)
LuxI and GFP behind a Bxb1 compatible genetic switch

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_R4030
BBa_R4030 Version 1 (Component)
PoPS/RiPS Generator composed of the Tet promoter and a strong RBS (R0040.E0030)

BBa_J329040
BBa_J329040 Version 1 (Component)
luxIR QS System with B0034 RBSs and LVA-tagged GFP

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_K584011
BBa_K584011 Version 1 (Component)
Lac-Lux hybrid promotor + CrtEBI + CI repressor + INP

BBa_I13273
BBa_I13273 Version 1 (Component)
YFP Producer Controlled by 3OC₆HSL Receiver Device

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

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.