Sequence Search | Advanced Search | SPARQL
Showing 6851 - 6900 of 6958 result(s)
Previous 133 134 135 136 137 138 139 140 Next



Public
BBa_K2150029
BBa_K2150029 Version 1 (Component)
pCon+RBS+tetR+DT+pTet+RBS+T7RNAP+Ter+RBS+pT7+tetX-GFP(fusion protein)+DT
Public
BBa_M1536
BBa_M1536 Version 1 (Component)
Thermal Hysteresis (Antifreeze) Protein (variant YL4) with 8-His tag with secretion tag and GFP
Public
BBa_K563010
BBa_K563010 Version 1 (Component)
Tor2 gene from the genome of the S. cerevisiae, central protein in TOR(target of rapamycin) pathway
Public
BBa_K2027009
BBa_K2027009 Version 1 (Component)
Control Sequence Peptide for Melanin Binding (Nonpolar-Protic)
Public
BBa_K2088006
BBa_K2088006 Version 1 (Component)
It encodes a kind of protein named 2Fe-2S ferredoxin, a 2Fe-2S iron-sulfur cluster binding domain. I
Public
iGEM 2019 Cell Fusion Protein of S-Layer SgsE and mCerulean
iGEM_2019_Cell2 Version 1 (Collection)

Public
iGEM 2019 Cell Fusion Protein of S-Layer SbpA and mCerulean
iGEM_2019_Cell4 Version 1 (Collection)

Public
iGEM 2019 Cell Fusion Protein of S-Layer SgsE and mCitrine
iGEM_2019_Cell1 Version 1 (Collection)

Public
iGEM 2019 Cell Low copy protein fusion vector (Silver lab standard)
iGEM_2019_Cell10 Version 1 (Collection)

Public
iGEM 2018 Cell Fusion Protein of S-Layer SbpA and mCerulean
iGEM_2018_Cell6 Version 1 (Collection)

Public
iGEM 2018 Cell Low copy protein fusion vector (Silver lab standard)
iGEM_2018_Cell13 Version 1 (Collection)

Public
iGEM 2018 Cell Fusion Protein of S-Layer SgsE and mCerulean
iGEM_2018_Cell4 Version 1 (Collection)

Public
iGEM 2018 Cell Fusion Protein of S-Layer SgsE and mCitrine
iGEM_2018_Cell3 Version 1 (Collection)

Public
BBa_K1051116
BBa_K1051116 Version 1 (Component)
Actin Targeting Protein
Public
BBa_M1174
BBa_M1174 Version 1 (Component)
protein1
Public
BBa_K1790001
BBa_K1790001 Version 1 (Component)
biosensor detect food allergens. A proteins conformation change in response to ligand binding couple
Public
BBa_K1790005
BBa_K1790005 Version 1 (Component)
biosensor detect food allergens. A proteins conformation change in response to ligand binding couple
Public
BBa_K1790000
BBa_K1790000 Version 1 (Component)
biosensors detect food allergens. A proteins conformation change in response to ligand binding coupl
Public
BBa_K1790003
BBa_K1790003 Version 1 (Component)
biosensor detect food allergens. A proteins conformation change in response to ligand binding couple
Public
BBa_K1790004
BBa_K1790004 Version 1 (Component)
biosensor detect food allergens. A proteins conformation change in response to ligand binding couple
Public
BBa_K1790002
BBa_K1790002 Version 1 (Component)
biosensor detect food allergens. A proteins conformation change in response to ligand binding couple
Public
PcotYZ
BBa_K823030 Version 1 (Component)
P<sub><i>cotYZ</i></sub>: <i>B. subtilis</i> promoter regulating expression of spore crust proteins
Public
BBa_K638201
BBa_K638201 Version 1 (Component)
Arabinose inducible Poly-His Reflectin A1 generator
Public
BBa_K1403001
BBa_K1403001 Version 1 (Component)
GFP generator in pSB1C3 under a weak promoter
Public
BBa_M45091
BBa_M45091 Version 1 (Component)
AGA1: Agglutinins, mating type specific cell surface Proteins, are synthesized by haploid cell of Sa
Public
BBa_K2018034
BBa_K2018034 Version 1 (Component)
phaCAB genes with additional promoter and RBS, that encodes proteins that can create PHB.
Public
BBa_K2018000
BBa_K2018000 Version 1 (Component)
phaCAB genes with additional promoter and RBS, that encodes proteins that can create PHB.
Public
BBa_K2018036
BBa_K2018036 Version 1 (Component)
phaCAB genes with additional promoter and RBS, that encodes proteins that can create PHB.
Public
BBa_K2018033
BBa_K2018033 Version 1 (Component)
phaCAB genes with additional promoter and RBS, that encodes proteins that can create PHB.
Public
BBa_K987000
BBa_K987000 Version 1 (Component)
This part is a coding part that produces Vip3Ca3, a protein that can deals with different forms of p
Public
enhanced
BBa_K2075011 Version 1 (Component)
enhanced Green fluorescenc protein (GFP)
Public
enhanced G
BBa_K2075012 Version 1 (Component)
enhanced Green fluorescenc protein (GFP)
Public
BBa_K1106010
BBa_K1106010 Version 1 (Component)
LuxI generator with strong RBS and double terminator
Public
BBa_J58009
BBa_J58009 Version 1 (Component)
Fusion protein Trg-EnvZ
Public
BBa_M11085
BBa_M11085 Version 1 (Component)
E coli outer membrane protein C (ompC) with BamHI RE site for insertion of gene to be expressed on o
Public
BBa_K1123017
BBa_K1123017 Version 1 (Component)
DNA Coding Sequence for EGFP Protein
Public
BBa_I721004
BBa_I721004 Version 1 (Component)
Lead Binding Protein + Promoter (version a)
Public
iGEM 2019 Cell Fusion Protein of S-Layer SbpA and mCherry RFP
iGEM_2019_Cell3 Version 1 (Collection)

Public
iGEM 2018 Cell Fusion Protein of S-Layer SbpA and mCherry RFP
iGEM_2018_Cell5 Version 1 (Collection)

Public
BBa_K125550
BBa_K125550 Version 1 (Component)
Protein Linker SSGSSG Library
Public
BBa_K204040
BBa_K204040 Version 1 (Component)
C<sub>4</sub>HSL generater
Public
BBa_K079021
BBa_K079021 Version 1 (Component)
LacI repressor and GFP reporter proteins under the control of the J23118 costitutive promoter and La
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.
Public
BBa_K145274
BBa_K145274 Version 1 (Component)
LuxI generator controlled by a AND-gate system.
Public
BBa_J133568
BBa_J133568 Version 1 (Component)
Protein Linker SSGSSG Library
Public
BBa_J133564
BBa_J133564 Version 1 (Component)
Protein Linker SSGSSG Library
Public
BBa_J133573
BBa_J133573 Version 1 (Component)
Protein Linker SSGSSG Library
Public
BBa_J133563
BBa_J133563 Version 1 (Component)
Protein Linker SSGSSG Library
Public
BBa_J133572
BBa_J133572 Version 1 (Component)
Protein Linker SSGSSG Library
Showing 6851 - 6900 of 6958 result(s)
Previous 133 134 135 136 137 138 139 140 Next