The largest database of trusted experimental protocols

Snu cell lines

Manufactured by Korean Cell Line Bank
Sourced in United States

SNU cell lines are a collection of human cell lines derived from various tissues and organs, developed and maintained by the Korean Cell Line Bank. The cell lines are characterized by their unique genetic profiles and biological properties, making them valuable tools for biomedical research and applications.

Automatically generated - may contain errors

2 protocols using snu cell lines

1

Establishing Cisplatin-Resistant Head and Neck Cancer Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
HNC cell lines (HN2–10) and SNU cell lines were purchased from the Korea Cell Line Bank (Seoul, Republic of Korea) and authenticated by short tandem repeat-based DNA fingerprinting and multiplex polymerase chain reaction (PCR). The cells were cultured in Eagle's minimum essential medium or Roswell Park Memorial Institute (RPMI) 1640 (Thermo Fisher Scientific, Waltham, MA, USA) with 10% fetal bovine serum at 37 °C in a humidified atmosphere containing 5% CO2. Normal oral keratinocytes or fibroblasts were obtained from patients undergoing oral surgery and used for in vitro assays. Three cisplatin-resistant HNC cell lines (HN3-cisR, HN4-cisR, and HN9-cisR) were developed from the parental HN3, HN4, and HN9 cells, respectively, by subjecting them to continuous exposure of increasing cisplatin concentrations [30] (link). The half-maximal inhibitory concentrations (IC50) of cisplatin (Sigma-Aldrich, St. Louis, MO, USA) in the parental (2.2–3.5 µM) and cisplatin-resistant (25.5–38.9 µM) HNC cells were determined using cell viability assays.
+ Open protocol
+ Expand
2

Cell Culture Maintenance Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Hep3B, PLC/PRF/5 and HepG2 cell lines were purchased from American Type Culture Collection (Virginia, USA) and SNU cell lines from Korean Cell Line Bank (Seoul, Korea). Cells were routinely cultured in DMEM (Hep3B, PLC/PRF/5 and HepG2) or RPMI-1640 (SNUs) medium supplemented with 10% FBS and 100 units/mL P/S at 37°C humidified atmosphere of 5% CO2. Cells were subcultured at 1:2 to 1:4 ratios every 3 or 4 days avoiding confluence.
+ 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!