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All samples were cultured in blood culture media and subcultured into Brucella agar medium.
All samples were cultured under the same standardized culture conditions as described before [16], [66] [68].
Sputum samples were cultured on Lowenstein-Jensen (LJ) culture media.
Sputum smear microscopy positive samples were cultured on Lowenstein-Jensen (LJ) culture medium.
When both samples were cultured the agreement between the two sampling methods was good.
To inhibit DCV efflux in T cells, positive control samples were cultured with FTC.
Samples were cultured in either normal or osteogenic medium.
Samples were cultured up to 28 days in vitro.
Samples were cultured for streptococci, staphylococci, and gram-negative bacteria.
All milk samples were cultured using standard milk microbiological techniques and DNA was extracted.
In early-degenerated cartilage, abnormal [Ca2+]i activities in deep zone were seen when samples were cultured in both 0 mM and 4 mM [Ca2+]e environment.
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