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Showing 601 - 618 of 618 result(s)
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Public
BBa_M30012
BBa_M30012 Version 1 (Component)
OmpR controlled mRFP
Public
BBa_K594011
BBa_K594011 Version 1 (Component)
A device that can accepts the 3--O-C6-HSL and then produces 3-O-C12-HSL and ECFP reporter.
Public
BBa_K594014
BBa_K594014 Version 1 (Component)
A device that can accepts the 3--OH-C14:1-HSL and then produces 3-O-C6-HSL and GFP reporter.
Public
BBa_K116503
BBa_K116503 Version 1 (Component)
GFP under control of pOmpC promoter.R0082+E0240
Public
BBa_I733005
BBa_I733005 Version 1 (Component)
Produce GFP in presence of AHL
Public
BBa_I733004
BBa_I733004 Version 1 (Component)
Produce LacZ alpha in response to AHL
Public
BBa_K549004
BBa_K549004 Version 1 (Component)
LacI promotor fused with the iron dependent regulator fur
Public
BBa_K1132014
BBa_K1132014 Version 1 (Component)
Promoter (OmpR, positive) followed by RFP protein generator
Public
BBa_J58102
BBa_J58102 Version 1 (Component)
Promoter activated by OmpR-P with the reporter GFP
Public
BBa_J58014
BBa_J58014 Version 1 (Component)
Promoter activated by OmpR-P with the reporter GFP
Public
BBa_K1452000
BBa_K1452000 Version 1 (Component)
Pos/neg selection (Bacillus)
Public
BBa_J58015
BBa_J58015 Version 1 (Component)
Mutated promoter activated by OmpR-P with the reporter GFP
Public
BBa_K1053203
BBa_K1053203 Version 1 (Component)
Pconst.-SRⅡ-HtrⅡ-EnvZ-Pompc-taRNA-DT-Pconst.-HHR-GFP-DT
Public
BBa_K1053202
BBa_K1053202 Version 1 (Component)
Pconst.-SRⅡ-HtrⅡ-EnvZ-Pompc-HHR-GFP-DT-Pconst.-taRNA-DT
Public
BBa_K1053204
BBa_K1053204 Version 1 (Component)
Pconst.-SRⅡ-HtrⅡ-EnvZ-Pompc-taRNA-DT-Pconst.-HHR*-GFP-DT
Public
BBa_R4030
BBa_R4030 Version 1 (Component)
PoPS/RiPS Generator composed of the Tet promoter and a strong RBS (R0040.E0030)
Public
BBa_K258003
BBa_K258003 Version 1 (Component)
Granulysin, a T Cell Product,Kills Bacteria by Altering Membrane Permeability
Public
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.
Showing 601 - 618 of 618 result(s)
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