Optimization of an E. coli L-rhamnose-inducible expression vector: test of various genetic module combinations.
about
Antibiotic-free selection in biotherapeutics: now and foreverTranslation initiation requires cell division cycle 123 (Cdc123) to facilitate biogenesis of the eukaryotic initiation factor 2 (eIF2).Plasmid addiction systems: perspectives and applications in biotechnology.Rhamnose-inducible gene expression in Listeria monocytogenes.Benzoic Acid-Inducible Gene Expression in Mycobacteria.Near-infrared fluorescent proteins for multicolor in vivo imaging.Far-red light photoactivatable near-infrared fluorescent proteins engineered from a bacterial phytochrome.A near-infrared BiFC reporter for in vivo imaging of protein-protein interactionsEngineering Genetically-Encoded Mineralization and Magnetism via Directed Evolution.The molecular toolbox for chromosomal heterologous multiprotein expression in Escherichia coli.Self-inducible Bacillus subtilis expression system for reliable and inexpensive protein production by high-cell-density fermentation.Improved soluble expression of the gene encoding amylolytic enzyme Amo45 by fusion with the mobile-loop-region of co-chaperonin GroES in Escherichia coliCharacterization of a mannose utilization system in Bacillus subtilis.Chondroitin Lyase from a Marine Arthrobacter sp. MAT3885 for the Production of Chondroitin Sulfate Disaccharides.A CGTase with high coupling activity using γ-cyclodextrin isolated from a novel strain clustering under the genus Carboxydocella.Synthetic biosensors for precise gene control and real-time monitoring of metabolitesAn enhanced recombinant amino-terminal acetylation system and novel in vivo high-throughput screen for molecules affecting α-synuclein oligomerisation.High-level intracellular expression of heterologous proteins in Brevibacillus choshinensis SP3 under the control of a xylose inducible promoter.CRISPR interference-guided multiplex repression of endogenous competing pathway genes for redirecting metabolic flux in Escherichia coli.Screening Fusion Tags for Improved Recombinant Protein Expression in E. coli with the Expresso® Solubility and Expression Screening System.Time-course and degradation rate of membrane scaffold protein (MSP1D1) during recombinant production.Development of a strictly regulated xylose-induced expression system in Streptomyces
P2860
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P2860
Optimization of an E. coli L-rhamnose-inducible expression vector: test of various genetic module combinations.
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Optimization of an E. coli L-r ...... s genetic module combinations.
@ast
Optimization of an E. coli L-r ...... s genetic module combinations.
@en
Optimization of an E. coli L-r ...... s genetic module combinations.
@nl
type
label
Optimization of an E. coli L-r ...... s genetic module combinations.
@ast
Optimization of an E. coli L-r ...... s genetic module combinations.
@en
Optimization of an E. coli L-r ...... s genetic module combinations.
@nl
prefLabel
Optimization of an E. coli L-r ...... s genetic module combinations.
@ast
Optimization of an E. coli L-r ...... s genetic module combinations.
@en
Optimization of an E. coli L-r ...... s genetic module combinations.
@nl
P2093
P2860
P356
P1433
P1476
Optimization of an E. coli L-r ...... s genetic module combinations.
@en
P2093
Angelika Wegerer
Josef Altenbuchner
Tianqi Sun
P2860
P2888
P356
10.1186/1472-6750-8-2
P577
2008-01-14T00:00:00Z
P5875
P6179
1044160674