The largest database of trusted experimental protocols

4 protocols using mhh nb 11

1

Neuroblastoma Cell Line Procurement and Culture

Check if the same lab product or an alternative is used in the 5 most similar protocols
Neuroblastoma cell lines (NBL) SKN-AS, SKN-SH, and SKN-BE(2)C were purchased from ATCC whereas NBL-S and MHH-NB-11 were purchased from DSMZ (Leibniz Institute DSMZ-German Collection of Microorganisms and Cell cultures, German). Cells were cultured as detailed in the Supplementary Methods.
+ Open protocol
+ Expand
2

Cell Line Characterization and Verification

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cell lines were grown according to the suppliers’ instructions at 37 °C in a 5%-CO2 humidified atmosphere. CHP-134, IMR-32, KELLY, LAN-1, SK-N-BE2 and −DZ were obtained from ECACC (Salisbury, UK). CHP-126, MHH-NB-11 and SIMA were obtained from DSMZ (Braunschweig, Germany). CHP-212 was obtained from ATCC. STA-NB-1, −7 and −10 were kindly provided by Dr. Peter F. Ambros (CCRI, Vienna, Austria). All cell lines were used at early passages (n = 3) to avoid the insurgence of any alteration, and all were checked for mycoplasma and other potential infections. All cell lines were checked against the Database of Cross-contaminated or Misidentified Cell Lines (http://iclac.org/), and none were found to have been previously flagged as cross-contaminated or misidentified.
+ Open protocol
+ Expand
3

Cell Line Authentication and Culturing Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
ES lines (MHH‐ES1, RD‐ES, SK‐ES1, SK‐N‐MC, and TC‐71), neuroblastoma lines (CHP126, MHH‐NB11, SHSY5Y, and SIMA), and pediatric human B‐cell precursor leukemic lines (cALL2, NALM6, and 697) were obtained from the German Collection of Microorganisms and Cell Cultures (DSMZ, Braunschweig, Germany). ES line VH64 was kindly provided by Marc Hotfilder (Münster University, Münster, Germany); osteosarcoma lines (HOS, HOS‐58, MG‐63, MNNG, SaOS, SJSA01, U2OS, and ZK‐58) by Jan Smida and Michaela Nathrath, Institute of Pathology and Radiation Biology (HMGU, Neuherberg, Germany). A673 was purchased from ATCC (LGC Standards, Teddington, UK). SB‐KMS‐KS1 and SB‐KMS‐MJ1 are ES cell lines that were established in our laboratory (Grunewald et al., 2012; Richter et al., 2009). Retrovirus packaging cell line PT67 was obtained from Takara Bio Europe/Clontech (Saint‐Germain‐en‐Laye, France). Cells were maintained in a humidified incubator at 37 °C in 5–8% CO2 atmosphere in RPMI 1640 or DMEM (both Life Technologies, Carlsbad, CA, USA) containing 10% heat‐inactivated fetal bovine serum (Biochrom, Berlin, Germany) and 100 μg·mL−1 gentamicin (Life Technologies). Cell lines were checked routinely for purity (e.g., EWS‐FLI1 translocation product, surface antigen or HLA phenotype) and mycoplasma contamination.
+ Open protocol
+ Expand
4

Neuroblastoma and Mesenchymal Stem Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
ES lines (SK-N-MC and TC-71), neuroblastoma lines (CHP126, MHH-NB11, SHSY5Y and SIMA) were obtained from the German Collection of Microorganisms and Cell Cultures (DSMZ, Braunschweig, Germany). A673 was purchased from ATCC (LGC Standards, Teddington, UK). Mesenchymal stem cell lines L87 an V54.2 were described previously [33 (link)]. Cells were maintained in a humidified incubator at 37°C in 5-8 % CO2 atmosphere in RPMI 1640 (Life Technologies, Carlsbad, CA, USA) containing 10 % heat-inactivated fetal bovine serum (Biochrom, Berlin, Germany) and 100 μg/ml gentamicin (Life Technologies). Cell lines were checked routinely for purity (e.g. EWS-FLI1 translocation product, surface antigen or HLA-phenotype) and Mycoplasma contamination.
+ 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!