BBa_K112223BBa_K112223 Version 1 (Component){a~ihfB!} The ihf beta gene ready to have rbs attached and stop codon, BBb format
BBa_K112211BBa_K112211 Version 1 (Component){a~int!} The integrase gene with rbs ready to be attached with stop codon, BBb format
BBa_K1332003BBa_K1332003 Version 1 (Component)The 5?? side of the intron(+exon fragment) from td gene of T4 phage without stop codon
xisBBa_K112204 Version 1 (Component){a~xis!} The bacteriophage lambda xis gene ready to have rbs attached and stop codon; assembly stand
BBa_K1351040BBa_K1351040 Version 1 (Component)pBS0K<i>Pspac</i>, an IPTG-inducible replicative expression vector for
BBa_J72117BBa_J72117 Version 1 (Component)BBb High copy entry vector, pBca1256
BBa_K1848001BBa_K1848001 Version 1 (Component)Human Gut Hormone Glucagon-like peptide 1 (7-37) (Sequence Lacks Stop Codon, but part possesses it)
BBa_K2074033BBa_K2074033 Version 1 (Component)pSB1C3-Cry11Aa(Codon optimization)+Extended FMDV 2A+Cyt1(Codon optimization)
BBa_K541715BBa_K541715 Version 1 (Component)Multi-host vector pTG262 converted to BioBrick vector wtih LALF protein and SacB signal peptide
BBa_K106693BBa_K106693 Version 1 (Component)AarI A!D acceptor vector (pRS315, Cyc1P, Adh1t)
BBa_K1114400BBa_K1114400 Version 1 (Component)This is a MoClo level 0 destination vector.
BBa_K1695013BBa_K1695013 Version 1 (Component)Riboswitch + Bacteriophage 21 codon optimized R gene
BBa_K1695014BBa_K1695014 Version 1 (Component)Riboswitch + Bacteriophage 21 codon optimized Rz gene
BBa_K1695012BBa_K1695012 Version 1 (Component)Riboswitch + Bacteriophage 21 codon optimized S gene
BBa_K137021BBa_K137021 Version 1 (Component)GFP with (AC)20 repeat after start codon
BBa_K1033204BBa_K1033204 Version 1 (Component)pSBLb4E15 E. coli and lactobacilli shuttle vector with erythromycin resistance
BBa_K1051356BBa_K1051356 Version 1 (Component)K1051301(clb2 promoter) + K1051053(K1051001 (non stop codon ECFP + K1051006 (Stop codon + TBY-1 term
BBa_K563053BBa_K563053 Version 1 (Component)vector pYE, designed for inducible expression of recombinant proteins in S.cerevisivae.
BBa_K802003BBa_K802003 Version 1 (Component)Shuttle vector for <i> E. coli</i> and <i>B. subtilis</i>
BBa_J36852BBa_J36852 Version 1 (Component)Streptavidin, single-chain dimer (no start codon)
BBa_K1695042BBa_K1695042 Version 1 (Component)Riboswitch Bacteriophage 21 Codon Optimized Lysis Cassette S R Rz
BBa_K137033BBa_K137033 Version 1 (Component)Device with GFP with (AC)21 repeat after start codon
BBa_K1695049BBa_K1695049 Version 1 (Component)pL8-UV5 + Riboswitch Bacteriophage 21 Codon Optimized Lysis Cassette S R Rz
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.