The largest database of trusted experimental protocols

3 protocols using dulbecco s modified eagle s media

1

Cell Lines for Oesophageal and Pancreatic Cancer

Check if the same lab product or an alternative is used in the 5 most similar protocols
The human distal oesophageal adenocarcinoma cell lines, FLO-1 and KYAE-1, were purchased from European Collection of Cell Cultures (Salisbury, UK). The human pancreatic cancer cell line AsPc-1 was purchased from the American Type Culture Collection (Manassas, VA, USA). AsPc-1shTAK1 cells stably expressing small hairpin RNA sequences to knockdown the expression of TAK1 has been previously described in Melisi et al (2011) (link). Distal oesophageal adenocarcinoma and pancreatic cancer cell lines were maintained in RPMI 1640 and Dulbecco's modified Eagle's media (LONZA, Basel, Switzerland), respectively, supplemented with 10% heat-inactivated FBS, 20 mmol l−1 HEPES (pH 7.4), penicillin (100 UI ml−1), streptomycin (100 mg ml−1), and 4 mmol l−1 glutamine (ICN Biomedicals Ltd., Irvine, CA, USA) in a humidified atmosphere of 95% air and 5% CO2 at 37 °C. The TAK1 kinase activity was targeted using (5Z)-7-oxozeaenol TAK1 kinase selective inhibitor (TOCRIS bioscience, Bristol, UK). For in vitro assays, (5Z)-7-oxozeaenol was dissolved in 100% dimethyl sulfoxide (DMSO) at a stock concentration of 10 mM. Cell irradiation was performed using a GammaCell 40 irradiator (Best Theratronics Ltd., Ottawa, Canada) as previously described in Melisi et al, 2009 (link).
+ Open protocol
+ Expand
2

Cell Line Culture and Stable Transfection

Check if the same lab product or an alternative is used in the 5 most similar protocols
The 293T cells and HeLa S3 cell were grown in Dulbecco's modified Eagle's media (Lonza) supplemented with 10% fetal bovine serum, 1% ultraglutamine (Lonza) and 1% pen/strep (Lonza) at 37°C with 5% CO2. For large-scale purification, S3 cells were grown in Joklik media at 37°C in the absence of C02. Stable cell lines (eH3.1, eH3.2, eH3.3) were generated as described previously (15 (link)).
+ Open protocol
+ Expand
3

Microglia Cell Culture Protocols

Check if the same lab product or an alternative is used in the 5 most similar protocols
All the chemicals used in this study are commercially purchased and used without further purification. Lipofectamine (LPS) was purchased from Thermo Fisher (00‐4976‐93); Beta Amyloid (1–42) was procured from Anaspec (AS24224), Mammalian protein extraction reagent (MPER; #78 505)), EDTA, Protease inhibitor (78 425) were purchased from Thermo Fischer Scientific. For 2D cell culture, murine microglia BV2 cell was used, human microglia HMC3 and cultured in Dulbecco's modified Eagle's media (12‐707F; Lonza) supplemented with 10% fetal bovine serum (FBS), L‐Glutamine (25‐005‐Cl; Corning), and Penicillin/streptomycin (DE17‐602E; Lonza). Cells were cultured in a 37 °C incubator with water‐saturated air and a 5% CO2 atmosphere and splitting was done every 2–3 days using trypsin (BE17‐161E; Lonza).
+ 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!