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The antibacterial effect of silver nanoparticle-treated silk fabrics was tested against E. coli and S. aureus by using a shaking flask method according to the antibacterial standard of knitted products (FZ/T 73023-2006, China).
The aqueous solubility of DRDE-07 in simulated intestinal fluid (SIF) and simulated gastric fluid (SGF) was measured using a shaking flask method.
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The maximum biomass in the micro-bioreactor (6.1 g/l) was 1.7 times as compared to using a shake flask (3.6 g/l).
The cultivation continued in a batchwise manner under laboratory conditions at 22°C, using a shake flask equipped with a stirrer and containing a working volume of 0.6 L, gassed with a sterile mixture of H2 O2 CO2 in variable ratios.
Table 1 Lipophilicities of [ 68 Ga]DOTATATE and [ 68 Ga]HA-DOTATATE and their respective 177 Lu-labeled analogs Peptide log P O/PBS [68Ga]DOTATATE −3.69 [177Lu]DOTATATE −3.16 [68Ga]HA-DOTATATE −3.12 [177Lu]HA-DOTATATE −2.69 Partition coefficients (logP O/PBS) of the radioligands between PBS (pH 7.4) and n-octanol were determined using a shake flask method (n = 6) [13].
Static batch culture of Ecad-/ ES cells was found to be an ineffective process as the loose cell aggregates required dispersing every 24 h, therefore, we investigated whether Ecad-/ ES cells could be cultured using a shake flask bioreactor (Figure 2).
In this work, the solubility of cefoxitin acid in organic solvents (methanol, acetonitrile, ethanol, isopropanol, n-propanol and ethyl acetate), water and water-methanol mixtures was measured spectrophotometrically using a shake-flask method within the temperature range 278.15 303.15 K.
Antimicrobial activities of fiber samples were measured against Escherichia coli and Staphylococcus aureus using a shake-flask method (GB/T 20944.3-2008 [China]).
Data are means ± SD (n = 3) Lipophilicities (from n-octanol/PBS partition coefficients POW) were determined using a shake-flask method; values are means from n = 6 determinations Fig. 1 Schematic representation of the PSMA-I&T-based theranostic concept for the clinical management of PCa.
Log P values were determined using a shake-flask method as described previously [33].
We could not detect isoprene production in three phases using standard incubation in a shaking flask as has been described for B. subtilis 6051 grown in a bioreactor.
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