BBa_K1683002
BBa_K1683002 Version 1 (Component)
pBAD+Strong RBS+E. coli tolC signal sequence+P. mirabilis tolC

BBa_K201012
BBa_K201012 Version 1 (Component)
Trans-Repressor (7) sequence, to be used for T-REX device

BBa_K201011
BBa_K201011 Version 1 (Component)
Trans-Repressor (4) sequence, to be used for T-REX device

BBa_K094106
BBa_K094106 Version 1 (Component)
Plux-rbs-CI-terminator-plambda P(O-R12)-rbs-cheZ

BBa_K1801000
BBa_K1801000 Version 1 (Component)
This part encodes for Glucose Oxidase. It is optimized for P. pastors

BBa_K1997022
BBa_K1997022 Version 1 (Component)
P+R->sLuc-N->Zif-N->RBS->Zif-C->sLuc-C->TER

BBa_K1997016
BBa_K1997016 Version 1 (Component)
P+R->sGFP-N->Zif-N->RBS->Zif-C->sGFP-C->TER

BBa_K1997013
BBa_K1997013 Version 1 (Component)
P+R->sHRP-N->Zif-N->RBS->Zif-C->sHRP-C->TER

BBa_K1172203
BBa_K1172203 Version 1 (Component)
GldA - glycerol dehydrogenase from Escherichia coli with P T7 and RBS

BBa_K1172204
BBa_K1172204 Version 1 (Component)
GldA - glycerol dehydrogenase from Escherichia coli with P lacI and RBS

BBa_K863012
BBa_K863012 Version 1 (Component)
tthl laccase from T. thermophilus with constitutive promoter J23100, RBS and His-tag

BBa_K748005
BBa_K748005 Version 1 (Component)
P2+RBS+GFP+T. P2 can be activated by phosphorylated AgrA.

enhanced g
BBa_K2075018 Version 1 (Component)
eGFP

BBa_K748004
BBa_K748004 Version 1 (Component)
P3+RBS+GFP+T. P3 can be activated by phosphorylated AgrA.

BBa_I735007
BBa_I735007 Version 1 (Component)
Cloning CDS PHO80 mutated in EX-Ptet-S-rbsRFP-P "RFP reporter"

BBa_K1662000
BBa_K1662000 Version 1 (Component)
Construct 1 Bicistronic:PelB-CDA under tetR and GFP under P(Lac)IQ promoter

BBa_K1997019
BBa_K1997019 Version 1 (Component)
P+R->GFP10->Zif-N->RBS->Zif-C->GFP11->RBS->GFP1-9->TER

BBa_K415008
BBa_K415008 Version 1 (Component)
pLux/cI-OR : RBS-mCherry : Term : p(lac) IQ : luxR : Term : pLux

BBa_K1767010
BBa_K1767010 Version 1 (Component)
P(Lac)IQ RBS LuxR ter ter luxpR RBS eyfp ter ter

BBa_K415009
BBa_K415009 Version 1 (Component)
pLux/cI-OR : RBS-mCherry : Term : P(tetR) : RBS-luxR : Term : pLux

BBa_K1587005
BBa_K1587005 Version 1 (Component)
Butyrate synthesis pathway (BBa_1587004) without ccr gene regulated by constitutive promoter p(Bla)

IBMc334
IBMc334 Version 1 (Component)
pSB3T5(BsaI-)-PBAD(SapI-)-B30-mCherry*(1-192)-GAEY-e-NpuNcage-FKBP-T-cat-PBAD(SapI-)-RiboJ-BCD1-FRB-NpuCcage-CFNS-mCherry*(193-236)-H6-Ter

IBMc335
IBMc335 Version 1 (Component)
pSB3T5(BsaI-)-PBAD(SapI-)-B30-mCherry*(1-192)-GAEY-e-NpuNcage-acVHH-T-cat-PBAD(SapI-)-RiboJ-BCD1-acVHH-NpuCcage-CFNS-mCherry*(193-236)-H6-Ter

BBa_K318521
BBa_K318521 Version 1 (Component)
Encryption Lysis - pLock Lysis p(pH) Hin pBile Cre pCons ramA

BBa_J17000
BBa_J17000 Version 1 (Component)
G-alpha-olf

BBa_K1767009
BBa_K1767009 Version 1 (Component)
P(Lac)IQ RBS Aiia RBS LuxR ter ter luxpR RBS eyfp ter ter

BBa_K557000
BBa_K557000 Version 1 (Component)
CheZ: phosphatase which dephosphorylates CheY-P and thus plays an important role in E.Coli chemotaxi

BBa_K1159314
BBa_K1159314 Version 1 (Component)
TMD with N-terminal Signal Peptide of SERK Receptor from ''P. patens'' in RFC[25] N-Part

BBa_J72103
BBa_J72103 Version 1 (Component)
{araC-Pbad}{rbs.coi}{double terminator}{cin, no start, frameshift}{repL no start}{LPsit}{rbs.pacA}{T

BBa_J31016
BBa_J31016 Version 1 (Component)
part produces the RNA construct crRNA-RBS-GFPLVA-tt that can only be translated in the presence of t

BBa_K415007
BBa_K415007 Version 1 (Component)
pLux/cI-OR : RBS-mCherry : Term : pLux/cI-OR : RBS-luxI : Term : p(tetR) : RBS-luxR : Term

BBa_K987000
BBa_K987000 Version 1 (Component)
This part is a coding part that produces Vip3Ca3, a protein that can deals with different forms of p

BBa_K1675026
BBa_K1675026 Version 1 (Component)
P-atp2-B0034-lacz alpha

RBS-TetR-T
BBa_K079007 Version 1 (Component)
TetR protein with terminator and RBS

BBa_K1675023
BBa_K1675023 Version 1 (Component)
P-atp2 mutant 706-B0034-lacz alpha

BBa_K1675022
BBa_K1675022 Version 1 (Component)
P-atp2 mutant 317-B0034-lacz alpha

BBa_K1675025
BBa_K1675025 Version 1 (Component)
P-atp2 mutant 399-B0034-lacz alpha

BBa_K1675024
BBa_K1675024 Version 1 (Component)
P-atp2 mutant 389-B0034-lacz alpha

BBa_K1675020
BBa_K1675020 Version 1 (Component)
P-atp2 mutant 226-B0034-lacz alpha

BBa_K876016
BBa_K876016 Version 1 (Component)
plac-lacO-RBS-GFP-T-pTet-LacI

BBa_K896986
BBa_K896986 Version 1 (Component)
this is a gene about a T cell receptor

BBa_K258003
BBa_K258003 Version 1 (Component)
Granulysin, a T Cell Product,Kills Bacteria by Altering Membrane Permeability

BBa_J58014
BBa_J58014 Version 1 (Component)
Promoter activated by OmpR-P with the reporter GFP

SET
BBa_K1433011 Version 1 (Component)
Terminator-RFP-RBS-attB-P-attP-RBS-GFP-Terminator

BBa_J58015
BBa_J58015 Version 1 (Component)
Mutated promoter activated by OmpR-P with the reporter GFP

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

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.