The largest database of trusted experimental protocols

5 protocols using nugc2

1

Gastric Cancer Cell Line Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
We used GC cell lines, which were obtained from the Japanese Collection of Research Bioresources Cell Bank (Osaka, Japan) as follows: MKN1, MKN45, MKN74, NUGC2, NUGC3, NUGC4, and SC-6-JCK. The GC cell lines AGS, KATOIII, and N87 were purchased from the American Type Culture Collection (ATCC) (Manassas, VA, USA). The human intestinal epithelial cell line FHs74Int (ATCC) served as a nontumorigenic control. Primary GC tissues and corresponding noncancerous mucosal tissues were collected from 200 patients who underwent gastrectomy at Nagoya University Hospital between 2001 and 2014. None of the patients underwent preoperative chemotherapy.
The methods were carried out in accordance with relevant guidelines. The study protocol was approved by the Medical Ethics Committee of the Nagoya University Hospital, protocol No. 2014–0043. Informed consent was obtained from all patients. Written informed consent for the use of clinical samples and data, as required by the Institutional Review Board, was obtained from all patients.
+ Open protocol
+ Expand
2

Gastric Cancer Cell Line Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
GC cell lines, the differentiated type (AGS, IM95, MKN1, MKN7, MKN74 and N87) and the undifferentiated type (GCIY, KATO-III, MKN45, NUGC2, NUGC3, NUGC4, OCUM1 and SC-6-JCK), were obtained from the Japanese Collection of Research Bio Resources Cell Bank (Osaka, Japan) or the American Type Culture Collection (ATCC, Manassas, VA, USA). A control, non-tumorigenic epithelial cell line (FHs 74) was purchased from the ATCC. The cells were cultured at 37 °C in RPMI medium (Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% foetal bovine serum in an atmosphere containing 5% CO2. All cell lines were authenticated using the short tandem repeat PCR method by the Japanese Collection of Research Bio Resources Cell Bank before the study commenced.
+ Open protocol
+ Expand
3

Gastric Cancer Cell Lines and Tissues

Check if the same lab product or an alternative is used in the 5 most similar protocols
The GC cell lines GCIY, IM95, MKN1, MKN7, MKN45, MKN74, NUGC2, NUGC3, NUGC4, OCUM-1, and SC-6-JCK were obtained from the Japanese Collection of Research Bioresources Cell Bank (JCRB, Osaka, Japan). AGS, KATOIII, and N87 GC cell lines and a nontumorigenic epithelial cell line (FHs74) were acquired from the American Type Culture Collection (Manassas, VA, USA). Three hundred pairs of surgically resected GC and adjacent noncancerous tissues were obtained from patients who underwent gastrectomy. A freely available integrated dataset (n = 1065 GC patients) was accessed at http://kmplot.com/analysis/ [13 (link)].
+ Open protocol
+ Expand
4

Gastric Cancer Cell Line Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following human GC cell lines were obtained from the Japanese Collection of Research Bioresources (Osaka, Japan): MKN45 (JCRB0254); the luciferase stably expressing cell line MKN45-Luc (JCRB1379), NUGC-2 (JCRB0821), OCUM-1 (JCRB0192), and KATO-III (JCRB0611). AGS was purchased from the American Type Culture Collection (Manassas, VA, USA). Cell line identities were confirmed by DNA fingerprinting through short tandem repeat profiling.
+ Open protocol
+ Expand
5

Gastric Cancer Cell Line Culturing Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
The gastric cancer cell lines MKN74, MKN45, MKN1, NUGC-2, NUGC-3, NUGC-4, and KATO-III were purchased from the JCRB cell bank (Ibaraki, Osaka, Japan). The JR-St and HSC39 cell lines were purchased from Takara Bio (Otsu, Shiga, Japan). The NCI-N87 cell line was obtained from ATCC (Manassas, VA, USA). The TMK1 cell line was initially established by Ochiai et al. [18] . All cell lines were cultured at 37 °C in a humidified 5 % CO 2 incubator in RPMI (Sigma, St. Louis, MO, USA) medium supplemented with 10 % fetal bovine serum (FBS; Sigma), 10 mM L-glutamine (Sigma), 100 U/ml penicillin, and 100 lg/ml streptomycin (Sigma), except for NUGC-2 cells, which were grown in RPMI medium supplemented with 15 % FBS.
+ 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!