BBa_K1650009
BBa_K1650009 Version 1 (Component)
Composite carrying the Lac-inducible CDI-operon,constitutively expressed RFP

BBa_K590064
BBa_K590064 Version 1 (Component)
The FabBrick: FabH2, an enzyme for changing up fatty acid biosynthesis

BBa_K726007
BBa_K726007 Version 1 (Component)
T7 driven lac operated inducer for the las quorum-sensing system

BBa_K1228003
BBa_K1228003 Version 1 (Component)
the device secrete Rabies virus strain ERA glycoprotein in bacillus subtilis

BBa_K2122100
BBa_K2122100 Version 1 (Component)
Device expressing the Gb3 Synthase enzyme under control of a constitutive promoter

BBa_K078007
BBa_K078007 Version 1 (Component)
2,3-dihydroxy-2,3-dihydrophenylpropionate dehydrogenase, the second step enzyme in PCBs degradation

BBa_K112219
BBa_K112219 Version 1 (Component)
{ihfB!} The ihf beta gene with start and stop codons, BBb format

SBOLDesigner CAD Tool
SBOLDesigner Version 3.0 (Agent)
SBOLDesigner is a simple, biologist-friendly CAD software tool for creating and manipulating the sequences of genetic constructs using the Synthetic Biology Open Language (SBOL) 2 data model. Throughout the design process, SBOL Visual symbols, a system of schematic glyphs, provide standardized visualizations of individual parts. SBOLDesigner completes a workflow for users of genetic design automation tools. It combines a simple user interface with the power of the SBOL standard and serves as a launchpad for more detailed designs involving simulations and experiments. Some new features in SBOLDesigner are SynBioHub integration, local repositories, importing of parts/sequences from existing files, import and export of GenBank and FASTA files, extended role ontology support, the ability to partially open designs with multiple root ComponentDefinitions, backward compatibility with SBOL 1.1, and versioning.

BBa_K1025003
BBa_K1025003 Version 1 (Component)
Thu-E Mutation Part

BBa_I745006
BBa_I745006 Version 1 (Component)
TRE-Bax-IRES2-EGFP

BBa_K1675009
BBa_K1675009 Version 1 (Component)
a device to produce alkali and neutralize the external acidic environment

BBa_K1657005
BBa_K1657005 Version 1 (Component)
It is called BAG. It have the resistance to glyphosate and glufosinate

BBa_K1189016
BBa_K1189016 Version 1 (Component)
GFP with a K coil under the control of a lacI promoter

BBa_K1657007
BBa_K1657007 Version 1 (Component)
It is called GAB. It have the resistance to glyphosate and glufosinate

BBa_K363006
BBa_K363006 Version 1 (Component)
A characterized calcium dependent response element binding site for the Crz1 activator

BBa_M11403
BBa_M11403 Version 1 (Component)
Type 1 promoter of the cpcBA operon in Synechocystis sp. PCC 6803

BBa_K1465229
BBa_K1465229 Version 1 (Component)
Sedoheptulose 1,7-bisphosphatase (glpX) from Bacillus methanolicus under the control of ptac

BBa_K1954001
BBa_K1954001 Version 1 (Component)
Lycopene cassette under the control of NarK, an oxidative stress inducible promoter

BBa_K1918100
BBa_K1918100 Version 1 (Component)
TRE-Kozak-EBFP2N(1-154)

BBa_M1353
BBa_M1353 Version 1 (Component)
thl + sigA promoter/consensus RBS

BBa_J58012
BBa_J58012 Version 1 (Component)
Promoter activated synergistically by cI and CRP with the reporter RFP

Excel2SBOL
Excel2SBOL_collection Version 1 (Collection)
A collection of sbol that is used for the excel2sbol library

BBa_M34014
BBa_M34014 Version 1 (Component)
Nucleotide sequence of a cDNA clone of saxiphilin from the liver of Rana Catesbeiana

BBa_K391001
BBa_K391001 Version 1 (Component)
Construct for characterization of P2 activity in the presence of AIP.

BBa_K391000
BBa_K391000 Version 1 (Component)
Construct for characterization of P2 activity in the presence of AIP.

BBa_I737007
BBa_I737007 Version 1 (Component)
Constitutive expression of all the accessory parts needed for our plasmid

BBa_I745007
BBa_I745007 Version 1 (Component)
TRE-Bak-IRES2-EGFP

GFP-AID
BBa_K812110 Version 1 (Component)
GFP fusion with the ubuquitinase E3 OsTirI recoginition domain for PSC2+ plasmid

BBa_J119315
BBa_J119315 Version 1 (Component)
Scaffold 2.0 for J-GGA (With the promoter between Junction A and B)

BBa_K078002
BBa_K078002 Version 1 (Component)
A fragment that encodes an enzyme involed in dioxin degradation, the third step

BBa_K1180002
BBa_K1180002 Version 1 (Component)
fusion protein of lamp 2b and RVG for brain targeting of the exosome

BBa_K1363005
BBa_K1363005 Version 1 (Component)
R0082-HfiA the HfiA protein express passway which can be regulated by light

BBa_K1963002
BBa_K1963002 Version 1 (Component)
A template for expression of sRNA fusions to the E. coli micC hairpin

BBa_K1551000
BBa_K1551000 Version 1 (Component)
To generate delta-4 fatty acid Desaturase so as to synthesize the DHA.

BBa_K812012
BBa_K812012 Version 1 (Component)
OsTirI Ubiquitinase E3 for AID tagged protein degradation in the presence of auxin

BBa_K078004
BBa_K078004 Version 1 (Component)
2，2???，3-Trihydroxybiphenyl 1,2-dioxygenase. The second step enzyme in dixon degradati

SBOL Compliant Software
SBOLCompliantSoftware_collection Version 1 (Collection)
A collection of software that supports the Synthetic Biology Open Language (SBOL) standard

pBAD-GFP
BBa_K845000 Version 1 (Component)
iGEM 2012 Grenoble Team proposes a new design and application to the pBAD promoter(paraBAD).

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

Intein_assisted_Bisection_Mapping
Intein_assisted_Bisection_Mapping_collection Version 1 (Collection)
Split inteins are powerful tools for seamless ligation of synthetic split proteins. Yet, their use remains limited because the already intricate split site identification problem is often complicated by the requirement of extein junction sequences. To address this, we augmented a mini-Mu transposon-based screening approach and devised the intein-assisted bisection mapping (IBM) method. IBM robustly revealed clusters of split sites on five proteins, converting them into AND or NAND logic gates. We further showed that the use of inteins expands functional sequence space for splitting a protein. We also demonstrated the utility of our approach over rational inference of split sites from secondary structure alignment of homologous proteins. Furthermore, the intein inserted at an identified site could be engineered by the transposon again to become partially chemically inducible, and to some extent enabled post-translational tuning on host protein function. Our work offers a generalizable and systematic route towards creating split protein-intein fusions and conditional inteins for protein activity control.

c-di-AMP
BBa_K1045002 Version 1 (Component)
CFP Reporter under control of the c-di-AMP-dependent YdaO Riboswitch

BBa_K2122000
BBa_K2122000 Version 1 (Component)
Device expressing the Gb3 Synthase enzyme under control of an arabinose inducible promoter

BBa_K2055016
BBa_K2055016 Version 1 (Component)
Part designed for verification and characterization of the FUR/LacI inverter

BBa_K078005
BBa_K078005 Version 1 (Component)
2，2???，3-Trihydroxybiphenyl 1,2-dioxygenase. The second step enzyme in dixon degradati

BBa_K1918102
BBa_K1918102 Version 1 (Component)
TRE-Kozak-EBFP2C(155-238)

BBa_K1918104
BBa_K1918104 Version 1 (Component)
TRE-Kozak-IntC:EBFP2C(155-238)

BBa_K1918101
BBa_K1918101 Version 1 (Component)
TRE-Kozak-EBFP2N(1-154)

BBa_K112212
BBa_K112212 Version 1 (Component)
{rbs.int!} The integrase gene with native rbs site and stop codon, BBb format