The largest database of trusted experimental protocols

2 protocols using mes sa

1

Cell Line Authentication and Cultivation

Check if the same lab product or an alternative is used in the 5 most similar protocols
SK-UT-1, SK-UT-1B, and MES-SA cells were purchased from American Type Culture Collection. SK-LMS-1 cells were provided by Sebastian Bauer (West German Cancer Center, Essen). Cell line identity and purity were verified using the Multiplex Cell Authentication and Contamination Tests (Multiplexion). All cell lines were regularly tested for mycoplasma contamination using the Venor GeM Mycoplasma Detection Kit (Minerva). Cell lines were cultured as follows: SK-LMS-1 in RPMI-1640 (Life Technologies), 15% FBS; SK-UT-1 and SK-UT-1B in MEM (Life Technologies), 10% FBS; MES-SA in McCoy’s medium, 10% FBS. All media were supplemented with 1% penicillin/streptomycin and 1% L-glutamine (Biochrom).
+ Open protocol
+ Expand
2

Characterization of Human Cancer Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
The human uterine sarcoma cell lines MES-SA and the doxorubicin selected MES-SA/Dx5 were obtained from ATCC (MES-SA: No. CRL-1976™, MES-SA/Dx5: No. CRL-1977™). The human mammary carcinoma cell lines MCF7, T47D, MDA-MB-231, MDA-MB-468, Hs578T, BT-549, the mouse leukemic P388 and its doxorubicin selected subline P388/ADR were obtained from the National Cancer Institute's Developmental Therapeutics Program (National Institutes of Health). P388/ADR, and Dx5 cells were maintained in 800 and 500 nmol/L doxorubicin (Adriamycin), respectively. The human breast cancer and the mouse leukemia cell lines were cultured in RPMI media (Life Technologies) supplemented with 10% fetal bovine serum, 5 mmol/L glutamine, and 50 units/mL penicillin and streptomycin (Life Technologies). MES-SA and MES-SA/Dx5 cells were cultured in supplemented DMEM media (Life Technologies). The chicken DT40 B cell line was grown in RPMI-1640 medium supplemented with 7% fetal bovine serum, 3% chicken serum, 50 μM 2-mercaptoethanol and penicillin/streptomycin. Wild-type DT40 clone18 cells [44] and a BRCA1 null mutant line [45] were used. All cell lines were cultured at 37 °C, 5% CO2.
+ 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!