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Showing 1951 - 1992 of 1992 result(s)
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Public
BBa_J69523
BBa_J69523 Version 1 (Component)
Const CFP reporter
Public
BBa_K1075003
BBa_K1075003 Version 1 (Component)
Promoter(const.)-AraC-Term-pBAD-RBS34 (Arabinose inducable promoter system)
Public
BBa_J06103
BBa_J06103 Version 1 (Component)
tetR repressible ECFP reporter
Public
BBa_J06003
BBa_J06003 Version 1 (Component)
tetR repressible ECFP reporter
Public
BBa_S04522
BBa_S04522 Version 1 (Component)
LuxI with RFP reporter
Public
BBa_K1960001
BBa_K1960001 Version 1 (Component)
Reporter controlled by sensing device
Public
BBa_K594011
BBa_K594011 Version 1 (Component)
A device that can accepts the 3--O-C6-HSL and then produces 3-O-C12-HSL and ECFP reporter.
Public
BBa_K137021
BBa_K137021 Version 1 (Component)
GFP with (AC)20 repeat after start codon
Public
BBa_K594014
BBa_K594014 Version 1 (Component)
A device that can accepts the 3--OH-C14:1-HSL and then produces 3-O-C6-HSL and GFP reporter.
Public
PL GFP
BBa_K193000 Version 1 (Component)
GFP reporter regulated by CI.
Public
BBa_K1845000
BBa_K1845000 Version 1 (Component)
RFP Reporter/Screening plasmid intermediate
Public
BBa_I20100
BBa_I20100 Version 1 (Component)
RBS Scaffold with GFP reporter
Public
BBa_I23000
BBa_I23000 Version 1 (Component)
RBS Scaffold with mCherry reporter
Public
BBa_K1893026
BBa_K1893026 Version 1 (Component)
J23119-ts-sfGFP -Gp2(star reporter)
Public
BBa_I719022
BBa_I719022 Version 1 (Component)
cI promoter with GFP reporter
Public
BBa_J92001
BBa_J92001 Version 1 (Component)
Lead Remover and Reporter Device
Public
BBa_J133001
BBa_J133001 Version 1 (Component)
RFP Reporter Cassette B0034.E1010.B0015
Public
BBa_K1676100
BBa_K1676100 Version 1 (Component)
GFP Reporter with pLac as promoter
Public
Pr+RFP
BBa_S03473 Version 1 (Component)
Lambda-system Pr promoter with RFP reporter
Public
BBa_K1778005
BBa_K1778005 Version 1 (Component)
eGFP:enhanced Green Fluorescent Protein. It???s the mutant of GFP. It is widely used as report gene
Public
BBa_K233306
BBa_K233306 Version 1 (Component)
YcdB - This part is a export tag that utilizes the Twin Arginine Transport pathway(TAT)
Public
BBa_J69591
BBa_J69591 Version 1 (Component)
GFP reporter device - using Standard Promoter (1RPU)
Public
BBa_K775012
BBa_K775012 Version 1 (Component)
diacetyl chimeric GPCR with Fus1-EGFP reporter (2)
Public
BBa_K779121
BBa_K779121 Version 1 (Component)
Short DNA reporter top strand (with RQ quencher) MammoBlock
Public
BBa_K779116
BBa_K779116 Version 1 (Component)
Short RNA reporter bottom strand (with ROX fluorophore) MammoBlock
Public
BBa_K1952012
BBa_K1952012 Version 1 (Component)
Hydrazine Synthase subunit alpha (Kust-2861) with LacZ reporter
Public
BBa_K1606010
BBa_K1606010 Version 1 (Component)
Kumamax enzyme that gluten updated m-cherry reporter device
Public
BBa_K395102
BBa_K395102 Version 1 (Component)
GFP reporter repressed by LuxR and 3OC6HSL (K395005:K121013)
Public
BBa_K395103
BBa_K395103 Version 1 (Component)
GFP reporter repressed by LuxR and 3OC6HSL (K395006:K121013)
Public
BBa_J58014
BBa_J58014 Version 1 (Component)
Promoter activated by OmpR-P with the reporter GFP
Public
BBa_K1114500
BBa_K1114500 Version 1 (Component)
MoClo Level 1 RFP reporter with AE fusion sites
Public
BBa_K812130
BBa_K812130 Version 1 (Component)
Citrine reporter with a Kozak sequence for expression in Xenopus
Public
Pr+CFP-
BBa_S03475 Version 1 (Component)
Lambda-system Pr promoter with CFP(no degradation tag) reporter
Public
BBa_J58015
BBa_J58015 Version 1 (Component)
Mutated promoter activated by OmpR-P with the reporter GFP
Public
BBa_K137033
BBa_K137033 Version 1 (Component)
Device with GFP with (AC)21 repeat after start codon
Public
pCMV-ECFP-
BBa_I763023 Version 1 (Component)
LacI coding device with ECFP as a reporter regulated by pCMV
Public
BBa_K779120
BBa_K779120 Version 1 (Component)
RNA Reporter top strand with quencher (RQ) and tag fluorophore (Alexa 488) MammoBlock
Public
BBa_K1088052
BBa_K1088052 Version 1 (Component)
GFP reporter with flexible linker at N-terminus for creation of GFP fusions
Public
PrtDEF
BBa_K258007 Version 1 (Component)
Export of recombinant proteins in Escherichia coli using ABC transporter of Erwinia chrysanthemi
Public
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.
Public
BBa_K079051
BBa_K079051 Version 1 (Component)
LacI repressor and GFP reporter proteins controlled by the J23118 promoter and Lac 1 operator
Public
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.
Showing 1951 - 1992 of 1992 result(s)
Previous 35 36 37 38 39 40