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We further performed growth assay on more complex media.
We performed growth selections upon an E. coli genome library developed using a moderate selection pressure to identify genomic regions implicated in acetate toxicity and tolerance.
To investigate whether ZS1 isolate was capable of utilizing crude oil for growth, which was essential for its potential application of in situ bioremediation, we performed growth analysis of ZS1 isolate in MS medium supplemented with 1% crude oil as sole carbon source (Fig. 6a).
We performed growth curves by measuring the %eGFP+ cells with time in BHK-21 cell populations exposed to BAC+ viruses at low multiplicity (Fig. 3D).
To examine potential physiological changes in Anp32a-deficient cells, we performed growth curve analysis on early-passage mixed-bred Anp32a−/− embryo fibroblasts (Figure 5).
We first created and characterized libraries of mixed insert size (see Methods) and then performed growth selections on mixtures of such libraries.
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We, therefore, performed growth-mortality simulations using the available data on release dates and number of released individuals.
To investigate whether recombination indeed confers a growth disadvantage in the presence of a wild-type strain, we performed growth-inhibition experiments with the recombinant isolate 2001044 and strain B16B6.
What if we began using whatever means are at our disposal to start performing growth mindset interventions on everyone we cared about?
Synthetic medium [19] supplemented with pectin from apple (10 g/l) was used to perform growth assay on pectin.
We tested the ability of F. succinogenes to hydrolyze and/or utilize different polysaccharides by performing growth assays using a variety of substrates as shown in Table 1.
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