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Penicillin streptomycin solution

Manufactured by GE Healthcare
Sourced in United States, Austria

Penicillin-streptomycin solution is a sterile liquid that contains the antibiotics penicillin and streptomycin. It is commonly used in cell culture and other laboratory applications that require the prevention of bacterial contamination.

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22 protocols using penicillin streptomycin solution

1

Breast Cancer Cell Line Establishment and Culture

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MDA-MB-231 and BT549 human breast cancer cell lines were purchased from the American Type Culture Collection (ATCC). MDA-MB-231 and BT549 cells were cultured in Dulbecco's modified Eagle's medium (DMEM; Thermo Fisher Scientific, Inc.) supplemented with 10% fetal bovine serum (HyClone; GE Healthcare Life Sciences) and 1% penicillin-streptomycin solution (Thermo Fisher Scientific, Inc.) in a humidified atmosphere containing 5% CO2 at 37°C. MDA-MB-231/GEM cells were established through continuous exposure of MDA-MB-231 cells to increasing concentrations of gemcitabine (initial concentration, 12 nM; increased to 6 µM over 6 months; Sigma-Aldrich; Merck KGaA) at 37°C. After 6 months, gemcitabine resistance was confirmed by comparison of cell viability between MDA-MB-231/GEM and MDA-MB-231 cells in response to 6 µM gemcitabine. The immortal breast cell line MCF10A was purchased from ATCC and cultured in DMEM/F12 media with 10% horse serum, 20 ng/ml epidermal growth factor, 100 ng/ml cholera toxin, 0.01 mg/ml insulin, 500 ng/ml hydrocortisone (all from HyClone; GE Healthcare Life Sciences) and 1% penicillin-streptomycin solution in a humidified atmosphere containing 5% CO2 at 37°C.
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2

Culturing HEK293T and HCT-116 Cells

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HEK293T cells (ATCC) were cultured in Dulbecco’s modified Eagle’s medium (DMEM, Thermo Fisher Scientific). HCT-116 cells with the ZNF598 gene being knocked out and the parental HCT-116 cells were kindly provided by Prof. Eric Bennett from the University of California San Diego,17 (link) and the cells were also cultured in DMEM. All culture media except those employed for transfection were supplemented with 10% fetal bovine serum (FBS, Thermo Fisher Scientific) and 1% penicillin-streptomycin solution (GE Healthcare). The cells were maintained in a humidified atmosphere with 5% CO2 at 37 °C, with medium renewal every 2–3 days depending on cell density. For plasmid transfection, the cells were cultured in the same media except that no penicillin-streptomycin solution was added.
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3

Porcine alveolar macrophage cell culture

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The PAM cells were prepared from 7-week-old healthy piglets which were not identified by polymerase chain reaction as having ASFV, porcine circovirus, classical swine fever virus, or porcine respiratory and reproductive syndrome virus, and were seronegative for ASFV. Primary PAM cells were cultured in growth medium containing an RPMI 1640 medium (Gibco, Thermo Fisher Scientific, Waltham, MA, USA), 10% fetal calf serum (FCS; Gibco), and 1% penicillin-streptomycin solution (Gibco). The cells were cultured and incubated at 37°C in a 5% CO2 incubator. Pig red blood cells (Percoll, GE Healthcare, Chicago, IL, USA) were prepared and mixed in maintenance medium (MM) which contained RPMI 1640 medium and 1% penicillin-streptomycin solution, and were kept at 4°C before testing.
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4

Lung Cancer Cell Line Maintenance

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A549 and H460 human lung cancer cell lines were purchased from the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China) or the Shanghai Institute of Pharmaceutical Industry (Shanghai, China). RPMI-1640, fetal bovine serum, penicillin/streptomycin solution, trypsin and PBS were purchased from HyClone, GE Healthcare Life Sciences (Logan, UT, USA). A549 and H460 lung cancer cell lines were maintained at 37°C in a humidified atmosphere containing 5% CO2 in RPMI-1640 supplemented with 10% fetal bovine serum, 1% penicillin and 1% streptomycin.
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5

Culturing U2OS Osteosarcoma Cells

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U2OS human osteosarcoma cells (American Type Culture Collection) were grown in high glucose Dulbecco’s modified Eagle’s medium (American Type Culture Collection, Manassas, VA) supplemented with 10% fetal bovine serum (Mediatech Inc., Manassas, VA) and 1% penicillin/streptomycin solution (HyClone reagents from GE Healthcare Life Sciences, Pittsburgh, PA). Cells were cultured at 37°C in a humidified atmosphere with 5% CO2. During cell passaging, cells were checked for the presence of mycoplasma contamination using MycoFluor Mycoplasma detection kit (Thermo Fisher Scientific, Waltham, MA). Cell line authentication was performed at the University of Arizona Genetics Core (Tucson, AZ).
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6

Cell Culture Protocols for Various Cell Lines

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Primary rat mesenchymal stem cells (MM), mouse embryonic fibroblast cells (MEF), murine macrophage cells (Raw 264.7), African green monkey kidney cells (Vero), human renal carcinoma cells (Caki), human cervical adenocarcinoma cells (HeLa), human hepatocellular carcinoma cells (Huh7), human astroglia (SVG p12, ATCC®CRL-8621™), human lung fibroblasts, and human embryonic kidney cells (293T) were cultured in Dulbecco’s modified Eagle’s medium (DMEM) (Hyclone, GE Healthcare, Chicago, IL) supplemented with 10% fetal bovine serum (FBS) (Sigma, Saint Louis, MO), 1 × penicillin-streptomycin (P/S) solution (Genesee Scientific, San Diego, CA). Human mesenchymal stem cells (MSC) from adipose tissue were cultured in MSC medium complemented with 5% FBS, 1% of MSC growth supplement and 1% of P/S solution (ScienCell, Carlsbad, CA). Human lung carcinoma cells (A549) and human monocytic cells (THP-1) were cultured with RPMI-1640 (Hyclone, GE Healthcare, Chicago, IL) supplemented with 10% FBS, and 1 × penicillin-streptomycin solution. Primary human umbilical vein endothelial cells (HUVEC) were cultured in VascuLife VEGF complete media (Lifeline cell technology, Frederick, MD). All cells were cultivated at 37°C with 5% CO2.
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7

Isolation and Characterization of ASCs

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Isolated SVF cells from different groups were subcultured to the 3rd passage for obtaining ASCs. The cells were cultured in low-glucose DMEM (Thermo Fisher, Waltham, USA) containing 10% FBS and 1% penicillin–streptomycin solution (GE Healthcare, Freiburg, Germany) until the confluence was 90%. ASCs were identified using cytofluorometry analysis. For detailed method of flow cytometry, see Additional file 1.
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8

Cultivation of Human Liver Cancer Cells

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Supplied and authenticated by the Chinese Academy of Sciences, Shanghai, human LC cell strains SMMC-7721 and MHCC97 were cultivated in the 1640 complete medium (Gibco® Thermo Fisher Scientific Inc., Rockford, IL, USA) comprising 1% penicillin-streptomycin solution (Hyclone™, GE Healthcare Life Sciences, Utah, USA)+10% fetal bovine serum. The incubation was performed in a 5% CO2 incubator at 37°C in a humidified atmosphere.
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9

Culturing Human Ovarian Cancer Cells

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ES-2 cells (human ovarian cancer cell lines) purchased from the ATCC (Manassas, VA, USA) were cultured in DMEM (Dulbecco’s Modified Eagle’s Medium) which contains 10% fetal bovine serum and 1% penicillin-streptomycin solution (Hyclone, GE Healthcare, Little Chalfont, UK) at 37 °C in a humidified 5% CO2 incubator.
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10

Isolation of Skin Fibroblasts from Donors

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A 3-mm skin biopsy was collected from the forearm of healthy donors or PH1 patients at University Hospital of La Laguna (Tenerife, Spain) for fibroblast isolation. All donors signed an informed consent, and the study was approved by the Ethical Committee of the University Hospital of La Laguna (Tenerife, Spain). Biopsies were washed with DMEM (1X) with GlutaMAX (Gibco, Cat#61965) and incubated in this medium with 2mg/ml type IV collagenase (Sigma, Cat#C5138) and 1% penicillin/streptomycin solution (Sigma, Cat#P4333) overnight at 37°C. The epidermis layer was separated from the dermis and discarded. The piece of dermis was maintained in the medium with collagenase until completely dissociated. Cell suspension was centrifuged, and cell pellet was seeded with DMEM (1X) with GlutaMAX, supplemented with 10% HyClone Research Grade Fetal Bovine Serum (GE healthcare, Cat#SV30160.03) and 1% penicillin/streptomycin solution. Fibroblast growth appeared 7-14 days after initial plating and medium was replaced as necessary during this incubation period.
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