BBa_Z0294
BBa_Z0294 Version 1 (Component)
A1,A2,A3,boxA

BBa_K1072008
BBa_K1072008 Version 1 (Component)
Flag tag

BBa_K1366006
BBa_K1366006 Version 1 (Component)
Amp R promoter

BBa_K1362999
BBa_K1362999 Version 1 (Component)
iGEMHD tag

BBa_I741020
BBa_I741020 Version 1 (Component)
promoter to xylF without CRP and several binding sites for xylR

BBa_K086025
BBa_K086025 Version 1 (Component)
modified Lutz-Bujard LacO promoter,with alternative sigma factor σ28

BBa_K122002
BBa_K122002 Version 1 (Component)
pADH1 (truncated)

BBa_K1652000
BBa_K1652000 Version 1 (Component)
pPGK1Gx

BBa_J70592
BBa_J70592 Version 1 (Component)
RFC12 Constitutive Promoter

BBa_K1841011
BBa_K1841011 Version 1 (Component)
pUO19 promoter

CMV
BBa_K415514 Version 1 (Component)
pCMV L4R1 MammoBlock Entry Vector

BBa_K102909
BBa_K102909 Version 1 (Component)
TA11 gate from synthetic algorithm v1.1

BBa_K1334001
BBa_K1334001 Version 1 (Component)
A improved promoter activitated by formaldehyde.

BBa_K102912
BBa_K102912 Version 1 (Component)
TA12 plus pause sequence

BBa_K102910
BBa_K102910 Version 1 (Component)
TA12 gate from synthetic algorithm v1.1

BBa_K511002
BBa_K511002 Version 1 (Component)
minCMV-4xMnt Promoter MammoBlock

BBa_K1935002
BBa_K1935002 Version 1 (Component)
pUNC-119 : Neuron Specific Promoter of C.elegans

BBa_J31020
BBa_J31020 Version 1 (Component)
produces taRNA

BBa_I732086
BBa_I732086 Version 1 (Component)
[aTc] -> PoPS (version1)

BBa_K1778000
BBa_K1778000 Version 1 (Component)
CYC1TATA sequence is derived from the TATA box secific sequence of yeast Saccharomyces cerevisiae

BBa_K1587004
BBa_K1587004 Version 1 (Component)
Butyrate synthesis pathway regulated by constitutive promoter p(Bla)

BBa_K1497027
BBa_K1497027 Version 1 (Component)
Scaffold (G-P)

BBa_K835002
BBa_K835002 Version 1 (Component)
cytoplasmic region of tar

Prm +
BBa_I12010 Version 1 (Component)
Modified lamdba Prm promoter (repressed by p22 cII)

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_K1395000
BBa_K1395000 Version 1 (Component)
nrfA gene (Nitrite reductase enzyme) under constitutive promoter

BBa_K112405
BBa_K112405 Version 1 (Component)
Promoter for CadA and CadB genes

BBa_K112406
BBa_K112406 Version 1 (Component)
cadC promoter

BBa_J54014
BBa_J54014 Version 1 (Component)
Surrfix_BglII,MluI(TokyoStanderd)

BBa_J54013
BBa_J54013 Version 1 (Component)
Prefix_SalI, BamHI(TokyoStanderd)