Sequence Search | Advanced Search | SPARQL
Showing 1301 - 1318 of 1318 result(s)
Previous 22 23 24 25 26 27



Public
BBa_I754001
BBa_I754001 Version 1 (Component)
ech protein generator for vanillin biosynthesis
Public
BBa_I769106
BBa_I769106 Version 1 (Component)
ech protein generator for vanillin biosynthesis
Public
BBa_K175049
BBa_K175049 Version 1 (Component)
GFP generator with "normal" RBS (B0034)
Public
BBa_K2123116
BBa_K2123116 Version 1 (Component)
Universal promoter for both phase of growth in tandem with downstram mer operator + RFP (K081014)
Public
BBa_K091119
BBa_K091119 Version 1 (Component)
LacI protein generator with a pTet promoter
Public
BBa_I534160
BBa_I534160 Version 1 (Component)
aiiA (LVA-) protein generator driven by pBad
Public
BBa_K638201
BBa_K638201 Version 1 (Component)
Arabinose inducible Poly-His Reflectin A1 generator
Public
BBa_K1403001
BBa_K1403001 Version 1 (Component)
GFP generator in pSB1C3 under a weak promoter
Public
BBa_K1132014
BBa_K1132014 Version 1 (Component)
Promoter (OmpR, positive) followed by RFP protein generator
Public
BBa_K584023
BBa_K584023 Version 1 (Component)
Ice Neucleating Protein Generator (RBS + InaZ [K584021] + Terminator)
Public
BBa_I769103
BBa_I769103 Version 1 (Component)
Feruloyl-CoA hydratase for vanillin biosynthesis protein generator
Public
BBa_K584022
BBa_K584022 Version 1 (Component)
Ice Neucleating Protein Generator (RBS + InaZ [K584021] + Terminator)
Public
BBa_K204040
BBa_K204040 Version 1 (Component)
C<sub>4</sub>HSL generater
Public
BBa_K511905
BBa_K511905 Version 1 (Component)
Repressible rtTA3 Transactivator Generator (Hef1a-LacO-rtTA3) MammoBlock Device
Public
BBa_K204022
BBa_K204022 Version 1 (Component)
3O<sub>6</sub>HSL generater device
Public
BBa_I718001
BBa_I718001 Version 1 (Component)
ech My new test generator part Feruloyl CoA hydratase for vanilin
Public
BBa_R4030
BBa_R4030 Version 1 (Component)
PoPS/RiPS Generator composed of the Tet promoter and a strong RBS (R0040.E0030)
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 1301 - 1318 of 1318 result(s)
Previous 22 23 24 25 26 27