BBa_K299500BBa_K299500 Version 1 (Component)Expression vector J23100+B0030
BBa_K299509BBa_K299509 Version 1 (Component)Expression Vector pT7+B0034
BBa_K1719014BBa_K1719014 Version 1 (Component)Constitutive promoter family member and RBS
BBa_I766223BBa_I766223 Version 1 (Component)HMTM1-EE under weak constitutive promoter
BBa_K311001BBa_K311001 Version 1 (Component)Strong and constitutive tet promoter with downstream mRFP
BBa_J13076BBa_J13076 Version 1 (Component)Monocistronic CFP/YFP expression cassette
placIQ RBSBBa_K193604 Version 1 (Component)GFP behind a constitutive promoter (placIQ) on pSB4A5
BBa_K2005051BBa_K2005051 Version 1 (Component)mCherry with T7 expression (oxidation-resistant)
BBa_K228816BBa_K228816 Version 1 (Component)Promoter(constitutive)+RBS(B0034)+tetR(C0040)+terminator(B0015)
BBa_K1323019BBa_K1323019 Version 1 (Component)Hfq expression cassette under a xylose inducible promoter
BBa_I719021BBa_I719021 Version 1 (Component)Constitutive 3OC<sub>6</sub>HSL Sender Device
BBa_K1438010BBa_K1438010 Version 1 (Component)Bacterial Iron Storage Expressor
BBa_J47053BBa_J47053 Version 1 (Component)Constitutive device (medium transcription) for lacI repressor, strong RBS
BBa_K346093BBa_K346093 Version 1 (Component)Constutitive promoter BBa_J23103+RBS(BBa_B0034)+PpbrR
BBa_K346009BBa_K346009 Version 1 (Component)Constutitive promoter(BBa_J23103)+RBS+MerR(BBa_K346001)
BBa_K1968010BBa_K1968010 Version 1 (Component)PgdaA constituve promoter from Aspergillus niger
BBa_K290001BBa_K290001 Version 1 (Component)constitutive RhlR with bicistronic LuxI - GFP controlled by pRhl
BBa_K332034BBa_K332034 Version 1 (Component)Constitutive promoter + 37℃ induced RBS + tetR + double terminator
BBa_K346078BBa_K346078 Version 1 (Component)Constutitive promoter BBa_J23109+pag activator(BBa_I746352)
BBa_K812132BBa_K812132 Version 1 (Component)mCFP with kozak sequence for expression in Xenopus
BBa_K812133BBa_K812133 Version 1 (Component)sfGFP with kozak sequence for expression in Xenopus
BBa_K079032BBa_K079032 Version 1 (Component)GFP reporter protein under the control of the BBa_J23100 constitutive promoter
BBa_K812130BBa_K812130 Version 1 (Component)Citrine reporter with a Kozak sequence for expression in Xenopus
BBa_K563053BBa_K563053 Version 1 (Component)vector pYE, designed for inducible expression of recombinant proteins in S.cerevisivae.
pSBBs0KBBa_K823026 Version 1 (Component)pSB<sub>Bs</sub>0K-P<sub>spac</sub> (replicative Bacillus subtilis expression vector; IPTG inducible
BBa_K1968013BBa_K1968013 Version 1 (Component)PgdaA constituve Phytobrick promoter: Glyceraldehyde-3-phosphate dehydrogenase from Aspergillus nige
Bacillus subtilis Collectionbsu_collection Version 1 (Collection)This collection includes information about promoters, operators, CDSs and proteins from Bacillus subtilis. Functional interactions such as transcriptional activation and repression, protein production and various protein-protein interactions are also included.
SEGASEGA_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.