BBa_J119137
BBa_J119137 Version 1 (Component)
pClone Red - Device for Testing New Promoters via Golden Gate Assembly

BBa_K322128
BBa_K322128 Version 1 (Component)
Phycocyanobilin synthesis genes + Red light detection system (EYFP as reporter)

BBa_K1649002
BBa_K1649002 Version 1 (Component)
Red light sensor with TetR not gate and GFP reporter

BBa_K1791001
BBa_K1791001 Version 1 (Component)
Standard RBS expressing MS2 Coat protein ribozyme affinity purification (RAP)

BBa_K1791002
BBa_K1791002 Version 1 (Component)
Low RBS expressing MS2 Coat protein ribozyme affinity purification (RAP)

BBa_K511812
BBa_K511812 Version 1 (Component)
CI434-VP16-Inducible Red Fluorescence Generator (minCMV-1xCI434-mKate) MammoBlock Device

BBa_K511824
BBa_K511824 Version 1 (Component)
Inducible Red Fluorescent Ligand Generator (UAS-Gal4-Delta-mCherry) MammoBlock Device

BBa_K511813
BBa_K511813 Version 1 (Component)
Mnt-VP16-Inducible Red Fluorescence Generator (minCMV-4xMnt-mKate) MammoBlock Device

BBa_K511806
BBa_K511806 Version 1 (Component)
Repressible Red Fluorescent Ligand Generator (Hef1a-LacO-Delta-mCherry) MammoBlock Device

BBa_K511814
BBa_K511814 Version 1 (Component)
Inducible Red Fluorescent Ligand Generator (TRE-Tight-Delta-mCherry) MammoBlock Device

BBa_J119384
BBa_J119384 Version 1 (Component)
rClone Red: Device for GGA Cloning and Testing RBS elements and Riboswitches

BBa_K106672
BBa_K106672 Version 1 (Component)
AarI AD acceptor vector (pRS305, Gal1P, Adh1t)

BBa_K1132017
BBa_K1132017 Version 1 (Component)
For the characterisation of the red light responsive system, under tetR regulation

BBa_J119361
BBa_J119361 Version 1 (Component)
tClone Red: Device for Testing Transciptional Terminators and Riboswitches via Golden Gate Assembly

Cyc1P Acce
BBa_K106014 Version 1 (Component)
AarI AD acceptor vector (pRS315, Cyc1P, Adh1t)

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_J119388
BBa_J119388 Version 1 (Component)
rClone Tet Red: Device for GGA Cloning and Testing RBS elements and Riboswitches

BBa_K1613012
BBa_K1613012 Version 1 (Component)
QsrR Binding Site inhibits the transcription and translation of Red Fluorescent Protein.

BBa_J100283
BBa_J100283 Version 1 (Component)
rClone Red with RBS: Device for GGA Cloning and Testing RBS elements and Riboswitches

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

BBa_K106670
BBa_K106670 Version 1 (Component)
AarI AD acceptor, pRS315, 8X LexAOPs Cyc1P, Adht1

BBa_K106698
BBa_K106698 Version 1 (Component)
AarI AD acceptor vector (pRS315, 8X LexAOps Fig1P, Adh1t)

BBa_K106697
BBa_K106697 Version 1 (Component)
AarI AD acceptor vector (pRS315, Cyc1P, Adh1t-8XLexA Ops)

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

Suppor Dev
BBa_K1433013 Version 1 (Component)
rT-rRFP-rRBS-attB-P-attP-RBS-lambda red-RBS-GFP-T-P-RBS-gp47-tag-T

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

BBa_K325239
BBa_K325239 Version 1 (Component)
Red Firefly Luciferase and LRE (under pBAD)<BR><i>L. Cruciata<BR>(E. coli optimised)</i>

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

SUPPORT DE
BBa_K1433022 Version 1 (Component)
rT-rKan-rRBS-attB-P-attP-RBS-lambda red-RBS-Chl-T-P-RBS-gp47-tag-T

BBa_K289009
BBa_K289009 Version 1 (Component)
pGADT7 is the AD Vector included with MATCHMAKER Two-Hybrid System 3.

BBa_K360115
BBa_K360115 Version 1 (Component)
Mutated red luciferase based on BBa_I712019

BBa_I720010
BBa_I720010 Version 1 (Component)
Ara landing pad (pBBLP 8)

BBa_K892000
BBa_K892000 Version 1 (Component)
Red light responsive luciferase

BBa_K133039
BBa_K133039 Version 1 (Component)
T7-CF-UREB-RGD-Histop

BBa_J119395
BBa_J119395 Version 1 (Component)
tClone Red containing the RS3 Riboswitch

BBa_K133037
BBa_K133037 Version 1 (Component)
T7-CF213-UB33-CF215-RGD-Histop

BBa_K892999
BBa_K892999 Version 1 (Component)
red light responsive inverter driving luciferase

BBa_K133020
BBa_K133020 Version 1 (Component)
CMV-CF213-multiHP-CF215-RGD-Histop (term.)

BBa_K133023
BBa_K133023 Version 1 (Component)
CMV-ss-CF213-multiHP-CF215-RGD-Histop (term)

Adh1P Acce
BBa_K106006 Version 1 (Component)
AarI AD acceptor vector (pRS315, Adh1P, Adh1t)

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.