BBa_J119308
BBa_J119308 Version 1 (Component)
pSB1A2-BR-HS-C-RNA-I

BBa_K497017
BBa_K497017 Version 1 (Component)
Reverse primer for Agrobacterium tumefaciens bacteriophytochrome gene for insertion after heme oxyge

BBa_M1680
BBa_M1680 Version 1 (Component)
Standard parts assembly for detection of high glucose levels using FAS promoter

BBa_K1072019
BBa_K1072019 Version 1 (Component)
pGAL1 + Brho + Flag + odr-10 + GFP +ADH1 Te + pFUS1 + BFP + ADH1 Te

BBa_K325239
BBa_K325239 Version 1 (Component)
Red Firefly Luciferase and LRE (under pBAD)<BR><i>L. Cruciata<BR>(E. coli optimised)</i>

BBa_K1716002
BBa_K1716002 Version 1 (Component)
NahR Biosensor for detection of acetylsalicylic acid/aspirin with blue chromoprotein reporter

BBa_M45905
BBa_M45905 Version 1 (Component)
Composite part for fluorescent detection of botulinum neurotoxin A (BoNT A)

BBa_K325109
BBa_K325109 Version 1 (Component)
EPIC Firefly Luciferase and LRE (under pBAD)<BR><i>P. Pyralis<BR>(E. coli optimised)</i>

KanR-AB-Bf
BBa_K349011 Version 1 (Component)
KanR-AB-BfuAI (for construction of AB BioBytes 2.0)

BBa_K1899000
BBa_K1899000 Version 1 (Component)
<i>tetp</i>-BFP-<i>phlFp</i>-RFP-<i>lacp</i>-GFP

BBa_K1480019
BBa_K1480019 Version 1 (Component)
pSB3C5 + MID + BF + AF TALEN (K1480001) Target sites

BBa_J119310
BBa_J119310 Version 1 (Component)
pSB1A2-BR-HS-G-IT-GGTT-RNA-I

BBa_K1480012
BBa_K1480012 Version 1 (Component)
pSB1C3 + BF and AF TALEN (K1480001) Target sites

BBa_K1480018
BBa_K1480018 Version 1 (Component)
pSB3C5 + AF and BF TALEN (K1480001) Target sites

BBa_K1480009
BBa_K1480009 Version 1 (Component)
pSB1C3 + MID and BF TALEN (K1480001) Target sites

BBa_K1615064
BBa_K1615064 Version 1 (Component)
HerE fused to CBDclos driven by LacI promoter

BBa_K1615062
BBa_K1615062 Version 1 (Component)
HerE fused to CBDcex driven by LacI promoter

BBa_K608001
BBa_K608001 Version 1 (Component)
First of two requisite genes required for the biosynthesis of phycocyanobilin from heme combined wit

BBa_K1480008
BBa_K1480008 Version 1 (Component)
pSB1C3 + MID, AF and BF TALEN (K1480001) Target sites

BBa_K1366101
BBa_K1366101 Version 1 (Component)
Genetic construct for lpp gene deletion (C1)

BBa_K1462520
BBa_K1462520 Version 1 (Component)
GAL1+YFP+SH3-lig+ADH1+GAL1+GFP+PDZ-lig+ADH1+GAL1+BFP+GBD-lig+ADH1

BBa_K1615060
BBa_K1615060 Version 1 (Component)
HerE fused to Linker+dCBD driven by LacI promoter

BBa_M45102
BBa_M45102 Version 1 (Component)
Cobalt detection Biobrick. RFP made in presence of Cobalt. Note the receptor also works in the prese

BBa_K1452000
BBa_K1452000 Version 1 (Component)
Pos/neg selection (Bacillus)

BBa_J119061
BBa_J119061 Version 1 (Component)
pSB1A2-BR

BBa_J119309
BBa_J119309 Version 1 (Component)
pSB1A2-BR-HS-G-RNA-I

BBa_K1497014
BBa_K1497014 Version 1 (Component)
Pelargonidin producing operon (low yield)- T7-B0034-F3H-B0034-DFR-B0034-ANS

KanR-BA-Bf
BBa_K349012 Version 1 (Component)
KanR-BA-BfuAI (for construction of BA BioBytes 2.0)

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.