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Aseptic operations may be validated by means of process simulation tests using microbial growth media, which are then incubated and examined for microbial contamination (media fill tests).
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One severe difficulty for investigating the roles of calcium is that many microorganisms, including the model filamentous ascomycete fungus Aspergillus nidulans, require only minute quantities of calcium, easily satisfied by trace contamination of media components.
After the selected treatment time, cells were washed twice with PBS to avoid external SL contamination from media and further analysis performed by the Lipidomics Core Facility of the Medical University of South Carolina (http://www.musc.edu/BCMB/lipidomics/index.shtml) as described previously [ 22, 24].
MGIT media contamination rates varied with sample type with routine slaughter surveillance granulomas having a 1.3 times higher contamination rate compared to fresh/frozen and high risk samples.
Additionally, corrosion associated material losses often produce contamination of surrounding media.
Three different categories of hazards were taken into account: acute and long-term hazard for humans, damage to ecosystems, environmental media contamination.
Anthropogenic chemicals, engineered antibiotics, excessive hormone use, and vast areas of natural arsenic pollution coupled with microbial contamination require special media for purification.
Yet, this powder metallurgy route poses several challenges: nanodiamond presents intrinsically difficult bonding with copper; contamination by milling media must be closely monitored; and full densification and microstructural homogeneity should be obtained with consolidation.
After plating the AECs on the culture insert at a density of 1.8 × 106 cells/cm2, the medium was changed every 2 or 3 days with fresh DMEM containing 10 % FBS for 7, 14, or 21 days, while avoiding contamination between the media in the upper and lower wells.
After plating the AECs at a density of 1.8 × 106 cells/cm2 (2 × 106 cells/Transwell), the medium was changed every 2 or 3 days with fresh DMEM containing 10 % FBS for 7 or 21 days, while avoiding contamination between the media in the upper and lower wells.
The presence of pyoverdine in water and body fluids samples can be directly linked to the presence of the Pseudomonas bacteria, thus being a nontoxic and low cost marker for the detection of water pollution as well as for the biological contamination of other media.
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