| P50 | author | Natalie J Saez | Q58237102 |
| P2093 | author name string | Renaud Vincentelli | |
| | Hervé Nozach | |
| | Marilyne Blemont | |
| P2860 | cites work | Disruption of reducing pathways is not essential for efficient disulfide bond formation in the cytoplasm of E. coli | Q24600389 |
| | Protein production and purification | Q24635875 |
| | Structural basis for hijacking of cellular LxxLL motifs by papillomavirus E6 oncoproteins | Q27676238 |
| | Protein production by auto-induction in high density shaking cultures | Q27860514 |
| | Escherichia coli maltose-binding protein is uncommonly effective at promoting the solubility of polypeptides to which it is fused | Q28142404 |
| | The P1' specificity of tobacco etch virus protease | Q28205691 |
| | DNA-binding specificities of human transcription factors | Q28854562 |
| | Ligation-independent cloning of PCR products (LIC-PCR) | Q29618962 |
| | A synergistic approach to protein crystallization: combination of a fixed-arm carrier with surface entropy reduction. | Q30386218 |
| | The high-throughput protein sample production platform of the Northeast Structural Genomics Consortium | Q30392340 |
| | Chaperone-based procedure to increase yields of soluble recombinant proteins produced in E. coli | Q33287499 |
| | Gateway(®) recombinational cloning: a biological operating system | Q34036000 |
| | Rapid, reliable ligation-independent cloning of PCR products using modified plasmid vectors | Q34245452 |
| | High throughput screening identifies disulfide isomerase DsbC as a very efficient partner for recombinant expression of small disulfide-rich proteins in E. coli. | Q34680566 |
| | Production of recombinant disulfide-rich venom peptides for structural and functional analysis via expression in the periplasm of E. coli. | Q34718440 |
| | High-throughput automated refolding screening of inclusion bodies | Q36526252 |
| | Tuning different expression parameters to achieve soluble recombinant proteins in E. coli: advantages of high-throughput screening. | Q37875026 |
| | Expression in Escherichia coli: becoming faster and more complex. | Q38082868 |
| | RF cloning: a restriction-free method for inserting target genes into plasmids | Q40316010 |
| | Recent contributions in the field of the recombinant expression of disulfide bonded proteins in bacteria | Q41809225 |
| | Comparison of SUMO fusion technology with traditional gene fusion systems: enhanced expression and solubility with SUMO. | Q41941212 |
| | MARINE-EXPRESS: taking advantage of high throughput cloning and expression strategies for the post-genomic analysis of marine organisms | Q42737931 |
| | Screening optimized protein purification protocols by coupling small-scale expression and mini-size exclusion chromatography | Q42946547 |
| | Ion channel pharmacology under flow: automation via well-plate microfluidics | Q46425740 |
| | Automated expression and solubility screening of His-tagged proteins in 96-well format | Q46707736 |
| | Dual expression system suitable for high-throughput fluorescence-based screening and production of soluble proteins | Q46841242 |
| | High throughput construction and small scale expression screening of multi-tag vectors in Escherichia coli | Q46843940 |
| | The conformational quality of insoluble recombinant proteins is enhanced at low growth temperatures. | Q50713308 |
| | Recombinant protein expression and solubility screening in Escherichia coli: a comparative study. | Q51128586 |
| | High-throughput protein expression screening and purification in Escherichia coli. | Q54352780 |
| | The use of systematic N- and C-terminal deletions to promote production and structural studies of recombinant proteins. | Q54428502 |
| | New fusion protein systems designed to give soluble expression in Escherichia coli | Q73041803 |
| | Generating fusions to glutathione S-transferase for protein studies | Q73089732 |
| | Fusions to maltose-binding protein: control of folding and solubility in protein purification | Q73089741 |
| | Thioredoxin as a fusion partner for production of soluble recombinant proteins in Escherichia coli | Q73089746 |
| | Disulfide bond formation in periplasm of Escherichia coli | Q77745570 |
| | High-throughput expression screening and purification of recombinant proteins in E. coli | Q86677066 |
| P433 | issue | 89 | |
| P921 | main subject | venom | Q3386847 |
| | Escherichia coli | Q25419 |
| P304 | page(s) | e51464 | |
| P577 | publication date | 2014-07-30 | |
| P1433 | published in | Journal of Visualized Experiments | Q954500 |
| P1476 | title | High throughput quantitative expression screening and purification applied to recombinant disulfide-rich venom proteins produced in E. coli | |