The largest database of trusted experimental protocols
Sourced in United States

ATCC 10145 is a laboratory equipment item from the American Type Culture Collection. It is designed for the cultivation and maintenance of cell cultures and microorganisms. The core function of this product is to provide a controlled environment for the growth and study of various biological samples.

Automatically generated - may contain errors

3 protocols using atcc 10145

1

Antimicrobial and Biofilm Assays

Check if the same lab product or an alternative is used in the 5 most similar protocols
Pseudomanas aeruginosa, VRSA, MSSA and MRSE strains were obtained from the American Type Culture Collection (ATCC 700699, ATCC10145, ATCC 25,923 and ATCC 51,625, respectively; Manassas, VA, USA). A. baumannii and MRSA strains were obtained from the culture collection of the Göteburg University (CCUG; Gothenburg, Sweden) (CCUG 61,012 and CCUG 60578). S. epidermidis was obtained from the Belgian Co-ordinated Collections of Microorganisms (Belgium) (LMG 10474; Gent, Belgium).
For antimicrobial testing inoculums were prepared in Luria-Bertani Broth (LB; ThermoFisher Scientific, Waltham, MA, USA) and for biofilms assays in Tryptic Soy Broth (TSB, Biokar Diagnostics, Beauvais, France).
For cell-based assays human keratinocytes (HaCat) were obtained from Cell Line Services (Oppenheim, Denmark). For assays cells were cultured, at 37 °C in a humidified atmosphere of 95% air and 5% CO2, using Dulbecco’s Modified Eagle’s Medium (DMEM) with 4.5 g/L glucose, L-glutamine without pyruvate (Lonza, Verviers, Belgium) containing 10% foetal bovine serum (FBS, Biowest, Nuaillé, France) and 1% (v/v) Penicillin-Streptomycin-Fungizone (Lonza, Verviers, Belgium).
+ Open protocol
+ Expand
2

Culturing and Harvesting Pseudomonas aeruginosa

Check if the same lab product or an alternative is used in the 5 most similar protocols
P. aeruginosa ATCC 10145 [23 ] (American Type Culture Collection, Manassas, VA) and a clinical isolate of P. aeruginosa (obtained from active ulcerative keratitis) were used and grown under the same conditions. Strains were cultured in triplicate in 50 ml of salt modified Luria-Bertani (LB) broth and grown to stationary phase (OD600 nm approximately 1.0) with incubation at 37 °C and shaking at 250 × rpm. Cultures were harvested and washed three times with PBS (10 mM sodium phosphate, 150 mM sodium chloride, pH 7.4±0.2). Cells were collected by centrifugation at 6,000 ×g for 10 min at 4 °C. The resulting bacterial cell pellets were frozen and stored at −80 °C until processing.
+ Open protocol
+ Expand
3

Cultivation of Pseudomonas aeruginosa Strains

Check if the same lab product or an alternative is used in the 5 most similar protocols
The study utilized five strains of Pseudomonas aeruginosa: PAO1, ATCC 10145, ATCC 15442 from the American Type Culture Collection and DBM 3081, and DBM 3777 which were obtained from the Collection of Microorganisms of the Department of Biochemistry and Microbiology, UCT Prague. Glycerol cryopreserves of these strains were stored at −70 °C. These strains represent a wide range of phenotypes from a soil isolate to the most researched clinical isolate, PAO1.
Prior to each experiment, all P. aeruginosa strains were precultivated in a Luria–Bertani (LB) liquid medium at 37 °C for 24 hours to achieve the exponential growth phase. The cultivation was carried out in Erlenmeyer flasks with a volume of 100 mL and agitation at 150 rpm.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!