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Showing 401 - 417 of 417 result(s)
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Public
BBa_K360115
BBa_K360115 Version 1 (Component)
Mutated red luciferase based on BBa_I712019
Public
BBa_I735007
BBa_I735007 Version 1 (Component)
Cloning CDS PHO80 mutated in EX-Ptet-S-rbsRFP-P "RFP reporter"
Public
BBa_J44008
BBa_J44008 Version 1 (Component)
pLac-RBS-HinLVA-TT-HixC-pBADrev-HixC-RBS-RE-TT-TetF
Public
BBa_J44006
BBa_J44006 Version 1 (Component)
pLac-RBS-HinLVA-TT-HixC-pBAD-HixC-RBS-TetF-TT-RE
Public
BBa_J44007
BBa_J44007 Version 1 (Component)
pLac-RBS-Hin-TT-HixC-pBADrev-HixC-RBS-RE-TT-TetF
Public
BBa_J44005
BBa_J44005 Version 1 (Component)
pLac-RBS-Hin-TT-HixC-pBAD-HixC-RBS-TetF-TT-RE
Public
BBa_K892000
BBa_K892000 Version 1 (Component)
Red light responsive luciferase
Public
BBa_J119395
BBa_J119395 Version 1 (Component)
tClone Red containing the RS3 Riboswitch
Public
BBa_I715069
BBa_I715069 Version 1 (Component)
Test part to see if RE and pLac +hixc can be expressed with GFP
Public
BBa_K892999
BBa_K892999 Version 1 (Component)
red light responsive inverter driving luciferase
Public
BBa_S03641
BBa_S03641 Version 1 (Component)
HixC : TetB-RBS<sub>rev</sub>-HixC
Public
BBa_S03638
BBa_S03638 Version 1 (Component)
HixC-pBad<sub>rev</sub>-HixC : RBS-TetF
Public
BBa_M11085
BBa_M11085 Version 1 (Component)
E coli outer membrane protein C (ompC) with BamHI RE site for insertion of gene to be expressed on o
Public
BBa_K779116
BBa_K779116 Version 1 (Component)
Short RNA reporter bottom strand (with ROX fluorophore) MammoBlock
Public
BBa_S03674
BBa_S03674 Version 1 (Component)
(-1,2) HixC-pBad<sub>rev</sub>-HixC : RBS-TetF-HixC
Public
BBa_J22121
BBa_J22121 Version 1 (Component)
Lac Y gene under the rec A(SOS) promoter in plasmid pSB2K3
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 401 - 417 of 417 result(s)
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