<p>Fluorescence was measured after 3(white bars) and with 10 µM (black bars) of chromate. The values represent averages and standard deviations of three replicates.</p
<p>Co-cultures of <i>E</i>. <i>coli</i> TD2158 and <i>S</i>. <i>enterica</i> (ratio = 1:10) (A) or <...
<p>Shown are normalized excitation and emission (A) and synchronous (B) fluorescence spectra of <i>E...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
<p>(A) Confocal images of <i>E</i>. <i>coli</i> transformed with GFP fusion plasmids. From left to r...
<p>0 h chromate incubation (⧫), 1 h chromate incubation (▪), 2 h chromate incubation (○), 3 h chroma...
<p>Cultures of exponential-growing cells of pCHRGFP1 <i>E. coli</i> and pCHRGFP2 <i>O. tritici</i> w...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
<p>(A) Fluorescence microscopy images corresponding to the Nile Red -stained strains <i>E</i>. <i>co...
<p><i>E. coli</i> transformants were cultured and diluted (from left to right) to an OD<sub>580</sub...
Background: Quantifying gene expression at single cell level is fundamental for the complete charact...
Reproducibility is a key challenge of synthetic biology, but the foundation of reproducibility is on...
Background: Quantifying gene expression at single cell level is fundamental for the complete charact...
Reproducibility is a key challenge of synthetic biology, but the foundation of reproducibility is on...
We constructed de novo a community of three model bacterial species, Vibrio cholerae, Staphylococcus...
<p>Cultures of (A) the MG1655 harboring pPro7(E)-<i>gfp</i> and (B) the JM1012 harboring the 3 plasm...
<p>Co-cultures of <i>E</i>. <i>coli</i> TD2158 and <i>S</i>. <i>enterica</i> (ratio = 1:10) (A) or <...
<p>Shown are normalized excitation and emission (A) and synchronous (B) fluorescence spectra of <i>E...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
<p>(A) Confocal images of <i>E</i>. <i>coli</i> transformed with GFP fusion plasmids. From left to r...
<p>0 h chromate incubation (⧫), 1 h chromate incubation (▪), 2 h chromate incubation (○), 3 h chroma...
<p>Cultures of exponential-growing cells of pCHRGFP1 <i>E. coli</i> and pCHRGFP2 <i>O. tritici</i> w...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
<p>(A) Fluorescence microscopy images corresponding to the Nile Red -stained strains <i>E</i>. <i>co...
<p><i>E. coli</i> transformants were cultured and diluted (from left to right) to an OD<sub>580</sub...
Background: Quantifying gene expression at single cell level is fundamental for the complete charact...
Reproducibility is a key challenge of synthetic biology, but the foundation of reproducibility is on...
Background: Quantifying gene expression at single cell level is fundamental for the complete charact...
Reproducibility is a key challenge of synthetic biology, but the foundation of reproducibility is on...
We constructed de novo a community of three model bacterial species, Vibrio cholerae, Staphylococcus...
<p>Cultures of (A) the MG1655 harboring pPro7(E)-<i>gfp</i> and (B) the JM1012 harboring the 3 plasm...
<p>Co-cultures of <i>E</i>. <i>coli</i> TD2158 and <i>S</i>. <i>enterica</i> (ratio = 1:10) (A) or <...
<p>Shown are normalized excitation and emission (A) and synchronous (B) fluorescence spectra of <i>E...
We present results of the first large-scale interlaboratory study carried out in synthetic biology, ...
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