Physical stimuli-responsive cell-free protein synthesis
نویسندگان
چکیده
منابع مشابه
Tetracycline Inhibition of Cell-Free Protein Synthesis
DAY, L. E. (Chas. Pfizer & Co., Inc., Groton, Conn.). Tetracycline inhibition of cell-free protein synthesis. II. Effect of the binding of tetracycline to the components of the system. J. Bacteriol. 92:197-203. 1966.-When tetracycline, an inhibitor of cell-free protein synthesis, was preincubated with each component of the Escherichia coli cell-free system, i.e., ribosomes, soluble ribonucleic ...
متن کاملTetracycline Inhibition of Cell-Free Protein Synthesis
DAY, L. E. (Chas. Pfizer & Co., Inc., Groton, Conn.). Tetracycline inhibition of cell-free protein synthesis. II. Effect of the binding of tetracycline to the components of the system. J. Bacteriol. 92:197-203. 1966.-When tetracycline, an inhibitor of cell-free protein synthesis, was preincubated with each component of the Escherichia coli cell-free system, i.e., ribosomes, soluble ribonucleic ...
متن کاملTetracycline Inhibition of Cell-Free Protein Synthesis
DAY, L. E. (Chas. Pfizer & Co., Inc., Groton, Conn.). Tetracycline inhibition of cell-free protein synthesis. II. Effect of the binding of tetracycline to the components of the system. J. Bacteriol. 92:197-203. 1966.-When tetracycline, an inhibitor of cell-free protein synthesis, was preincubated with each component of the Escherichia coli cell-free system, i.e., ribosomes, soluble ribonucleic ...
متن کاملMulti-Layered Films Containing a Biomimetic Stimuli-Responsive Recombinant Protein
Electrostatic self-assembly was used to fabricate new smart multi-layer coatings, using a recombinant elastin-like polymer (ELP) and chitosan as the counterion macromolecule. The ELP was bioproduced, purified and its purity and expected molecular weight were assessed. Aggregate size measurements, obtained by light scattering of dissolved ELP, were performed as a function of temperature and pH t...
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ژورنال
عنوان ژورنال: Synthetic and Systems Biotechnology
سال: 2020
ISSN: 2405-805X
DOI: 10.1016/j.synbio.2020.11.001