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Obtaining bacterial samples is crucial to ensure the detection and susceptibility testing of the causative pathogen.
Raman spectroscopy of bacterial samples is usually performed by a modified light microscopic device.
A limitation of the assay when running on complex bacterial samples is that the primers will have different efficiencies and dynamic ranges due to imperfect matches with some of the target sequences.
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For FTIR analysis bacterial samples were prepared according to Deokar et al. (2013).
Bacterial samples were isolated from the digesta collected from the omasum.
Bacterial samples were isolated from the wastewater and soil found at the Muteh gold mine (Isfahan-Iran).
After 12, 17.5 and 19 h of incubation, bacterial samples were centrifuged for 5 min at 11,600×g at 4 °C, and the precipitate was frozen.
Reactions with bacterial samples were incubated for 20 min instead of 10 min. Substrates included 1 ng biotinylated UCP2, and 300 ng mtRNA.
Eight fungal species and ten bacterial samples were isolated from drinking water supply PVC pipelines in Tirupati, Chittoor district, AP, India.
This resistance is highly problematic for effective therapeutic decisions, especially when considering that many resistance phenotypes are shut down when bacterial samples are isolated from patients and examined for clinical bacteriological phenotypes.
In this experiment, LB broth nutrient media were used, where at first UV vis absorption of shell-3/1D and 3D 3D Ag nano-assemblies were measured and then UV vis absorption of just bacterial samples was taken for comparative account.
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