BBa_K337056
BBa_K337056 Version 1 (Component)
synthetic binding site of miR 122 (imperfect) KD: 64%

BBa_K337053
BBa_K337053 Version 1 (Component)
synthetic binding site of shRNA miRhaat (imperfect) KD:69 %%

BBa_K337052
BBa_K337052 Version 1 (Component)
synthetic binding site of shRNA miRhaat (perfect) KD:97%

BBa_K337057
BBa_K337057 Version 1 (Component)
synthetic binding site of miR 122 (imperfect) KD: 24%

BBa_K337054
BBa_K337054 Version 1 (Component)
synthetic binding site of shRNA miRhaat (imperfect) KD:28%

BBa_K152007
BBa_K152007 Version 1 (Component)
Synthetic operon of CrtEBIY and FrdBCD and GFP

BBa_K1124107
BBa_K1124107 Version 1 (Component)
pLac-hpaBC-plambda-sRNA(anti-tyrR)-plambda-sRNA (anti-csrA) (L-DOPA synthesis device)

BBa_K1172304
BBa_K1172304 Version 1 (Component)
Riboflavin synthesis gene cluster from s. oneidensis under control of T7 promoter and strong RBS

Di
BBa_K1152004 Version 1 (Component)
Expression cassette for NRPS that synthesizes a Pro-Leu-Dipeptide

BBa_K1170001
BBa_K1170001 Version 1 (Component)
Synthetic construct superfolder green fluorescent protein (sfgfp) gene, complete cds

BBa_M1197
BBa_M1197 Version 1 (Component)
Ralstonia eutropha phasin (phaP)

BBa_M1297
BBa_M1297 Version 1 (Component)
Ralstonia Eutropha Phasin (PhaP)

BBa_M1012
BBa_M1012 Version 1 (Component)
Ralstonia eutropha phasin (phaP)

BBa_K258012
BBa_K258012 Version 1 (Component)
AI2-dependent KGF synthesis with RFP reporter and AHL production for Quaroum Sensin Death Mechanism

BBa_J329030
BBa_J329030 Version 1 (Component)
QS System with BBa_J329998 Synthetic RBS + Const. RFP Expression

BBa_K2123204
BBa_K2123204 Version 1 (Component)
Bioaccumulator device: Strong promoter + OmpA fused to Synthetic Phytochelatin + B0015

BBa_K2066117
BBa_K2066117 Version 1 (Component)
Synthetic Enhancer: 2x TetO Binding Cassette + NRII on UNS

BBa_K152005
BBa_K152005 Version 1 (Component)
Promoterless Synthetic Operon of CrtE,B,I,Y and GFP

BBa_K2066118
BBa_K2066118 Version 1 (Component)
Synthetic Enhancer with 3X TetO cassette (52s) on UNS backbone

BBa_K2066113
BBa_K2066113 Version 1 (Component)
Synthetic Enhancer with 2X TetO cassette (55as) on UNS backbone

BBa_K1051262
BBa_K1051262 Version 1 (Component)
The measurement pathway of degradation tag K1051208.

BBa_K1051260
BBa_K1051260 Version 1 (Component)
The measurement pathway of degradation tag K1051206.

BBa_K1051261
BBa_K1051261 Version 1 (Component)
The measurement pathway of degradation tag K1051207.

BBa_K2066114
BBa_K2066114 Version 1 (Component)
Synthetic Enhancer: 3x TetO Binding Cassette (52s) + NRII on UNS

BBa_K2066112
BBa_K2066112 Version 1 (Component)
Synthetic Enhancer Project: Ntr promoter driven NRII2302 (mut) on UNS Standard

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

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

BBa_K2066116
BBa_K2066116 Version 1 (Component)
Synthetic Enhancer Project: 3x TetO Binding Cassette (52s) + sfGFP on UNS

BBa_K2066115
BBa_K2066115 Version 1 (Component)
Synthetic Enhancer Project: 2x TetO Binding Cassette (55as) + sfGFP on UNS

BBa_K223021
BBa_K223021 Version 1 (Component)
SoxS + Part:BBa_K152005 (Promoterless Synthetic Operon of CrtE,B,I,Y and GFP)

BBa_K2066120
BBa_K2066120 Version 1 (Component)
Synthetic Enhancer Project: 3X TetO Binding Cassette(52S) + NRII + sfGFP on UNS

BBa_K2066119
BBa_K2066119 Version 1 (Component)
Synthetic Enhancer Project: 2X TetO Binding Cassette(52S) + NRII + sfGFP on UNS

BBa_K2066121
BBa_K2066121 Version 1 (Component)
Synthetic Enhancer Project: 2X TetO Binding Cassette(55aS) + NRII + TetR + sfGFP on UNS

BBa_K2066122
BBa_K2066122 Version 1 (Component)
Synthetic Enhancer Project: 3X TetO Binding Cassette(52S) + NRII + TetR + sfGFP on UNS

BBa_K809721
BBa_K809721 Version 1 (Component)
DLD3 promoter + kozak + hoiln(lambda phage) + ADH1 terminator

BBa_K300079
BBa_K300079 Version 1 (Component)
Phasin (PhaP) - head domain - with flexible protein domain linker downstream

BBa_K2123115
BBa_K2123115 Version 1 (Component)
Universal promoter (Tac + JK26) for both growth phase with downstream mer operator + K081014

BBa_K2123114
BBa_K2123114 Version 1 (Component)
Stationary phase promoter in tandem (3 repetition) with downstream mer operator + RFP (K081014)

BBa_M1002
BBa_M1002 Version 1 (Component)
Phasin-Complete coding sequence from Ralstonia eutropha, PHA granule-associated protein

BBa_K2123117
BBa_K2123117 Version 1 (Component)
Novel RFP device regulated by mercury: MerR (regulatory protein) + Stationary phase with mer operato

BBa_K2123116
BBa_K2123116 Version 1 (Component)
Universal promoter for both phase of growth in tandem with downstram mer operator + RFP (K081014)

iGEM Parts Registry
igem_collection Version 1 (Collection)
The iGEM Registry is a growing collection of genetic parts that can be mixed and matched to build synthetic biology devices and systems. As part of the synthetic biology community's efforts to make biology easier to engineer, it provides a source of genetic parts to iGEM teams and academic labs.

BBa_K2123301
BBa_K2123301 Version 1 (Component)
Novel Synthetic Phytochelatin codon optimized for E. coli expression

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.

SBOLDesigner CAD Tool
SBOLDesigner Version 3.1 (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 the ability to add variant collections to combinatorial derivations, enumerating those collections, and the ability to view sequence features hierarchically. There are also some small changes to the way that preferences work in regards to saving a design with incomplete sequences.

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.

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.