BBa_K1638030BBa_K1638030 Version 1 (Component)Leucine zipper fused to T25 domain of <i>cyaA</i> with cAMP-induced RFP generator
BBa_K1638031BBa_K1638031 Version 1 (Component)Leucine zipper fused to T18 domain of <i>cyaA</i> with cAMP-induced RFP generator
BBa_K2047001BBa_K2047001 Version 1 (Component)Fluorescent reporter system with stem-loop, GFP_Stem-loop with free energy of -25.6 kcal/mol
BBa_K1132037BBa_K1132037 Version 1 (Component)AND-inverted RFP gate (BBa_K1132034) with T7 polymerase under the control of a strong promoter
BBa_K1132038BBa_K1132038 Version 1 (Component)XOR-inverted RFP gate (BBa_K1132035) with T7 polymerase under the control of a strong promoter
BBa_K2082231BBa_K2082231 Version 1 (Component)RFP under the control of an optimized lacZ promoter combined with the protein SH2:cI434
BBa_K750008BBa_K750008 Version 1 (Component)Quorum sensing system based on LuxI and LuxR to control the expression of parts behind
pLacIQ+eGFBBa_K193207 Version 1 (Component)TmTHP with promotor for constituitive expression and with EGFP for fusion of Anti-Freeze Protein
T7+eGFP+TmBBa_K193208 Version 1 (Component)TmTHP with promotor for constituitive expression and with EGFP for fusion of Anti-Freeze Protein
BBa_K1361002BBa_K1361002 Version 1 (Component)Curli Fiber generator where CsgBtrunc, a dissociative nucleator, under the control of Pbad promoter
BBa_K1412600BBa_K1412600 Version 1 (Component)Endow the CL-1(E.coli engineered strain) the ability of chemotaxis and quorum sensing
BBa_J120030BBa_J120030 Version 1 (Component)Composite part with Yeast promoter,CH1 domain of human Ab, ADAM17 cleavage sequence & Phoratoxin.
BBa_K1363604BBa_K1363604 Version 1 (Component)key of no of RNA logic gates
BBa_K1861020BBa_K1861020 Version 1 (Component)Fusion protein of the TALE constant domain and a SpyTag in an expression cassette
BBa_K079021BBa_K079021 Version 1 (Component)LacI repressor and GFP reporter proteins under the control of the J23118 costitutive promoter and La
BBa_K1994022BBa_K1994022 Version 1 (Component)Multiple dCas9 binding sites with weak omega promoter upstream of GFP + dCas9 expression cassette
BBa_K2055015BBa_K2055015 Version 1 (Component)Promoter + Inverter with Ferric Uptake Regulator & LacI. Activates gene expression in presence of Fe
BBa_M45101BBa_M45101 Version 1 (Component)Composite biobrick intended to induce biofilm formation in the presence of lactose. Made from parts
LaLaLaBBa_K1479001 Version 1 (Component)0.0 Testing the UE of the bio-brick upload page, not designing a real one
BBa_K2055019BBa_K2055019 Version 1 (Component)Part designed for verification and characterization of the heat the shock promoter and Inverter.
BBa_K880001BBa_K880001 Version 1 (Component)Asymmetrically digestible reporter to assay the activity of DNA recombinases FimE K137007 and HbiF K
BBa_K2176001BBa_K2176001 Version 1 (Component)Cassette for the constitutive production of GAL4-KaiCp and LexA-SasA, linked by a self-cleaving P2A
BBa_K1216014BBa_K1216014 Version 1 (Component)BBa_K1216014 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL.
BBa_K1216012BBa_K1216012 Version 1 (Component)BBa_K1216012 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL.
BBa_K1216013BBa_K1216013 Version 1 (Component)BBa_K1216013 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL.
BBa_K1216011BBa_K1216011 Version 1 (Component)BBa_K1216007 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL.
BBa_K1216010BBa_K1216010 Version 1 (Component)BBa_K1216010 is a variant of the wild-type luxR promoter with a lowered sensitivity for LuxR-AHL. (
BBa_K185033BBa_K185033 Version 1 (Component)An inverter of a special lactose operon system based on J23110-rbs34-lacI-dter-plac-rbs31
BBa_K1361004BBa_K1361004 Version 1 (Component)Curli Fiber generator under the control of Pbad promoter with CsgA modified by His tag
BBa_K2082237BBa_K2082237 Version 1 (Component)RFP and Tetracycline resistence(tetA) under the control of a modified lacZ promoter; Fusion protein
BBa_K079049BBa_K079049 Version 1 (Component)GFP reporter protein under the control of the J23118 constitutive promoter and LexA 2 operator
Altered Sequence ActivitiesAlteredSequenceActivities_collection Version 1 (Collection)A set of activities to point to ways in which sequences have been altered between source and upload
BBa_K079020BBa_K079020 Version 1 (Component)GFP reporter under the control of J23118 promoter and Lac 2 operator auto-regulated by LacI protein
BBa_K1109007BBa_K1109007 Version 1 (Component)FepA L8T Mutant -composite of Large Diffusion pore for E. coli outer membrane coding sequence transc
BBa_K1778005BBa_K1778005 Version 1 (Component)eGFP:enhanced Green Fluorescent Protein. It???s the mutant of GFP. It is widely used as report gene
BBa_J31016BBa_J31016 Version 1 (Component)part produces the RNA construct crRNA-RBS-GFPLVA-tt that can only be translated in the presence of t
BBa_K2088006BBa_K2088006 Version 1 (Component)It encodes a kind of protein named 2Fe-2S ferredoxin, a 2Fe-2S iron-sulfur cluster binding domain. I
Bm3R1BBa_K1401000 Version 1 (Component)TetR homolog. This is a MoClo part of the Bm3R1 repressor gene with CD fusion sites ('AATG', 'AGGT')
sigA-P1BO_2991 Version 1 (Component) BBa_K1189029BBa_K1189029 Version 1 (Component)TALE-A with a his tag linked to a K coil under the control of a LacI promoter
BBa_M45102BBa_M45102 Version 1 (Component)Cobalt detection Biobrick. RFP made in presence of Cobalt. Note the receptor also works in the prese
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.