BBa_K1431834
BBa_K1431834 Version 1 (Component)
amajLime, yellow-green chromoprotein reporter system (Weak Promoter, Strong RBS)

BBa_K1431824
BBa_K1431824 Version 1 (Component)
amajLime, yellow-green chromoprotein reporter system (Weak Promoter, Weak RBS)

Xylr senso
BBa_I723140 Version 1 (Component)
Xylene sensor for creation of reporter constructs (secondary version)

BBa_K511817
BBa_K511817 Version 1 (Component)
Inducible Yellow Fluorescent Protein Generator (TRE-Tight-EYFP-FF4x4) MammoBlock Device

BBa_K511822
BBa_K511822 Version 1 (Component)
Inducible Yellow Fluorescent Protein Generator (UAS-Gal4-EYFP-FF4x4) MammoBlock Device

BBa_T9012
BBa_T9012 Version 1 (Component)
A mutant version of T9002 following a recombination event

BY-Toggle
BBa_K1908000 Version 1 (Component)
Blue-Yellow fluorescent protein toggle switch using pLac and OmpC promoter.

BBa_K1711001
BBa_K1711001 Version 1 (Component)
yeVenus-TheoA; coding sequence for enhanced yellow fluorescent protein and theophylline-sensative ap

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

BBa_K235024
BBa_K235024 Version 1 (Component)
[K235018][K235021] (mCherry generator, ribokey-mediated signal inversion)

BBa_I13213
BBa_I13213 Version 1 (Component)
BioBricked version of the natural Lux system with order reversed

BBa_K812051
BBa_K812051 Version 1 (Component)
Golden brick version of pSB1K3 plasmid for Golden Gate and Golden Brick cloning

pSB1C3 GB
BBa_K812050 Version 1 (Component)
Golden brick version of pSB1C3 plasmid for Golden Gate and Golden Brick cloning

BBa_K2097000
BBa_K2097000 Version 1 (Component)
CpxR binding site attached to a yellow-green color protein (YGCP) acts as a neutral pH indicator.

BBa_K1159117
BBa_K1159117 Version 1 (Component)
Red light triggered Kill Switch for plants translation unit (PhyB/PIF3 version)

BBa_K1159118
BBa_K1159118 Version 1 (Component)
Red light triggered Kill Switch for plants translation unit (PhyB/PIF6 version)

BBa_K235022
BBa_K235022 Version 1 (Component)
[K235018][K235019] (mCherry generator, pAra-controlled ribokey-mediated signal inversion)

BBa_J100272
BBa_J100272 Version 1 (Component)
rClone Red Version 2: Device for GGA Cloning and Testing RBS elements and Riboswitches

BBa_J100282
BBa_J100282 Version 1 (Component)
rClone Red Version 2 with RBS: Device for GGA Cloning and Testing RBS elements and Riboswitches

BBa_J100297
BBa_J100297 Version 1 (Component)
rClone Red Version 1.5 with RBS 2.0: Device for GGA Cloning and Testing RBS elements and Riboswitche

BBa_J100296
BBa_J100296 Version 1 (Component)
rClone Red Version 2 with RBS 2.0: Device for GGA Cloning and Testing RBS elements and Riboswitches

BBa_K1159120
BBa_K1159120 Version 1 (Component)
Red light triggered TEV Protease with FRET Reporter for plants translation unit (PhyB/PIF6 version)

BBa_K1159119
BBa_K1159119 Version 1 (Component)
Red light triggered TEV Protease with FRET Reporter for plants translation unit (PhyB/PIF3 version)

BBa_K235023
BBa_K235023 Version 1 (Component)
[K235018][K235020] (mCherry generator, pAra-controlled signal inversion)

BBa_K1903000
BBa_K1903000 Version 1 (Component)
dCas9 A version

BBa_I721004
BBa_I721004 Version 1 (Component)
Lead Binding Protein + Promoter (version a)

BBa_K783040
BBa_K783040 Version 1 (Component)
This is a MoClo converted version of BBa_J23110

BBa_K783034
BBa_K783034 Version 1 (Component)
This is a MoClo converted version of BBa_J23114

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.