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Salmonella typhimurium cicc21484

Sourced in United States

Salmonella typhimurium (CICC21484) is a bacterial strain maintained in the China Center of Industrial Culture Collection. It is a well-characterized microorganism commonly used in laboratory research and testing applications.

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2 protocols using salmonella typhimurium cicc21484

1

Salmonella and E. coli Strain Sourcing

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Standard strains of Escherichia coli (ATCC25922) and Salmonella choleraesuis (ATCC13312) were purchased from American Type Culture Collection (Manassas, VA, United States), Salmonella typhimurium (CICC21484) was purchased from the China Center of Industrial Culture Collection (Beijing, China), and Salmonella typhi suis (CVCC3783) was purchased from the China Veterinary Culture Collection Center (Beijing, China). Clinically resistant Salmonella strains (SP-JH-Y1407-52, SP-JH-Y1407-31, and SP-JH-Y1407-22) were donated by the Center for Agricultural Product Quality and Safety of Guangdong province (Guangdong, China).
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2

Antimicrobial Evaluation of Bacterial Strains and Skin Cell Culture

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Escherichia coli CICC 10003, Staphylococcus aureus CICC 10384, Listeria monocytogenes CMCC 54004, Salmonella typhimurium CICC 21484 were purchased from the China Center of Industrial Culture Collection (Beijing). Listeria monocytogenes CMCC 54004 was obtained from the College of Food Science and Technology, Yunnan Agricultural University (Kunming, Yunnan Province, China). Bacterial strains were conserved at -80°C in glycerol containing nutrient broth and were subcultured twice in Luria-Bertani broth medium under agitation (100 rpm) at 37°C for 24 h before use. The initial concentration of cells was adjusted to 10 6 cfu/mL by dilution in PBS (pH 7.4, containing 137 mM NaCl, 2.7 mM KCl, 10.1 mM Na 2 HPO 4 , and 1.8 mM KH 2 PO 4 , without calcium and magnesium) for subsequent experiments.
Human skin epithelial cells (HaCaT) were provided by the Moringa Institute of Yunnan Agricultural University. Cells were stored with 90% fetal bovine serum and 10% dimethyl sulfoxide at -80°C and cultured in RPMI 1640 medium containing 10% heat-inactivated fetal bovine serum (Hyclone Laboratories, Logan, UT) and 1% penicillin streptomycin antibiotic mixture (Gibco, Waltham, MA). All cell lines were cultured at 37°C in a humidified atmosphere at 5% CO 2 and 95% air.
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