BBa_K1361003
BBa_K1361003 Version 1 (Component)
Curli Fiber generator under the control of T7 promoter with a relatively strong expression of CsgA,C

BBa_K640004
BBa_K640004 Version 1 (Component)
Device for conjugation of plasmids from E. coli to pseudomonas

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.

BBa_K783045
BBa_K783045 Version 1 (Component)
This is a MoClo converted version of BBa_J23109

BBa_K783053
BBa_K783053 Version 1 (Component)
This is a MoClo converted version of BBa_E0040

BBa_K783043
BBa_K783043 Version 1 (Component)
This is a MoClo converted version of BBa_J23102

BBa_K783037
BBa_K783037 Version 1 (Component)
This is a MoClo converted version of BBa_J23118

BBa_K783042
BBa_K783042 Version 1 (Component)
This is a MoClo converted version of BBa_R0079

BBa_K783036
BBa_K783036 Version 1 (Component)
This is a MoClo converted version of BBa_J23117

BBa_K783052
BBa_K783052 Version 1 (Component)
This is a MoClo converted version of BBa_C0051

BBa_K783051
BBa_K783051 Version 1 (Component)
This is a MoClo converted version of BBa_B0034

BBa_K783047
BBa_K783047 Version 1 (Component)
This is a MoClo converted version of BBa_B0030

BBa_K783033
BBa_K783033 Version 1 (Component)
This is a MoClo converted version of BBa_J23113

BBa_K783041
BBa_K783041 Version 1 (Component)
This is a MoClo converted version of BBa_J23111

BBa_I733001
BBa_I733001 Version 1 (Component)
big toe

BBa_K1051284
BBa_K1051284 Version 1 (Component)
The RFP with degradation tag M0052

BBa_K152008
BBa_K152008 Version 1 (Component)
250 bp fragment from the Zea mays gene TB1

BBa_K581000
BBa_K581000 Version 1 (Component)
sgrS1+Terminator (small RNA regulator, conjugate part of ptsG1)

BBa_K1361001
BBa_K1361001 Version 1 (Component)
Curli Fiber generator under the control of T7 promoter with a relatively weak expression of CsgA,C

BBa_B0023
BBa_B0023 Version 1 (Component)
TE from coliphage T7, reversed

BBa_K416004
BBa_K416004 Version 1 (Component)
Aga2:(Gly3Ser)4 Linker Composite Part

BBa_K1918010
BBa_K1918010 Version 1 (Component)
TRE

BBa_T1008
BBa_T1008 Version 1 (Component)
Example part

BBa_K176237
BBa_K176237 Version 1 (Component)
Repressible cell density->PoPS: PoPS->tetR-LVA->K176085->PoPS

BBa_J85700
BBa_J85700 Version 1 (Component)
TRE-tight

BBa_K1058003
BBa_K1058003 Version 1 (Component)
Promoter of penicillinase blaZ as well as promoter of blaR1

BBa_K200005
BBa_K200005 Version 1 (Component)
OtsA: Part 1 of 2 for trehalose producing enzymes.

BBa_I20260
BBa_I20260 Version 1 (Component)
Measurement Kit Test of J23101

BBa_J70040
BBa_J70040 Version 1 (Component)
A BioScaffold Part (Uses AarI, MabI) for Library Vector Preparation (see Part Design page)

BBa_R4030
BBa_R4030 Version 1 (Component)
PoPS/RiPS Generator composed of the Tet promoter and a strong RBS (R0040.E0030)

BBa_K1753000
BBa_K1753000 Version 1 (Component)
the omega subunit of E.coli RNA polymerase with T7 promoter, RBS and terminator(BBa_B0014)

BBa_K233325
BBa_K233325 Version 1 (Component)
The complete turing machine construct

BBa_K310012
BBa_K310012 Version 1 (Component)
Composite part of golS with RBS and terminator.

BBa_K1510409
BBa_K1510409 Version 1 (Component)
A Steptococcus Mutants adhesive complex.

BBa_I12012
BBa_I12012 Version 1 (Component)
Reporter for the Barkai-Leibler oscillator

BBa_K1947023
BBa_K1947023 Version 1 (Component)
This part serves as a catch system expressed in <i>E. coli.

BBa_K1051801
BBa_K1051801 Version 1 (Component)
Targeted to HUBI gene ATG downstream position of the 12 bp sgRNA, cooperate to dCas 9 protein, inhib

BBa_K313007
BBa_K313007 Version 1 (Component)
gfp generator in the reverse direction

oriTr/LacZ
BBa_K125350 Version 1 (Component)
oriTr with lac promoter and lacZ

BBa_K196001
BBa_K196001 Version 1 (Component)
CcdA antidote with the mob promoter (forward)

BBa_I713001
BBa_I713001 Version 1 (Component)
A pBBR1MCS plasmid without the mob gene.

ccdA
BBa_K196000 Version 1 (Component)
CcdA antidote with the mob promoter (reverse)

BBa_K313001
BBa_K313001 Version 1 (Component)
DNA invertase hin in the reverse direction

BBa_K1555002
BBa_K1555002 Version 1 (Component)
The cueo promoter with a gfp reporter

BBa_K1323018
BBa_K1323018 Version 1 (Component)
oriV from the Staphylococcus aureus pSK41 Plasmid

BBa_K118012
BBa_K118012 Version 1 (Component)
Synthetic ribosome binding site added by Son of Babel procedure

xis/int
BBa_K112234 Version 1 (Component)
{rbs.xis.int!} The bacteriophage lambda xis/integrase gene with native rbs and stop codon; assembly

LMR
BBa_K175031 Version 1 (Component)
Lock for medium RBS (B0032) from the lock/key library TUD09

BBa_K1657002
BBa_K1657002 Version 1 (Component)
It is called TAB. It have the resistance to glyphosate and the 2, 4-Dichlorophenoxyacetic acid