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The CRL-2271 is a laboratory instrument designed for the culture and maintenance of cells. It provides a controlled environment for the growth and propagation of various cell lines. The core function of this product is to offer a reliable and consistent platform for cell culture applications.

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3 protocols using crl 2271

1

Culturing Human Neuroblastoma Cell Lines

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We used three human NB cell lines purchased from ATCC®: CRL22271 (SK-N-BE.2), CRL2266 (SH-SY5Y) and HTB11(SK-N-SH). CRL2266 and CRL2271 cells were cultured in 1:1 mixture of ATCC-formulated Eagle's Minimum Essential Medium (EMEM) and F12 Medium with 10% fetal bovine serum (FBS), 100 U/ml penicillin, and 10 μg/ml streptomycin. HTB11 cells were cultured in Eagle's Minimum Essential Medium (EMEM) containing 10% fetal bovine serum (FBS), 100 U/ml penicillin, and 10 μg/ml streptomycin. All cells were placed in a humidified atmosphere of 5% CO2 at 37°C and the medium was changed every 72 hours.
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2

Characterization of Neuroblastoma Cell Lines

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Five NB cell lines were purchased from ATCC (New York, NY). CRL-2267, CCL-127, CRL-2271 (of male origin) CRL-2266, and CRL- 2149 (of female origin) were cultured in Eagle's Minimum Essential Media (EMEM) (ATCC, Manassas, VA) supplemented with 10% heat inactivated Fetal Bovine Serum (FBS), and l-Glutamine-penicillin-streptomycin solution (designated complete media) (Sigma, St. Louis, MO) at 37 °C, 5% CO2. SMS-KCNR (of male origin) was purchased from Children's Oncology Group (Texas Tech University) and was cultured in RPMI-1640 (Sigma). Two terminally differentiated olfactory neuroblastoma cell lines, T-268 and JFEN, were a kind gift from Timothy J. Triche (Department of Pathology, Children's Hospital of Los Angeles, Los Angeles, CA 90027; 21). The stock cell cultures were grown in 25 mL or 75 mL flasks (Thermo-Scientific, Nunc, Rochester, NY). ZIKV strains PRVABC59 and MR 766 were provided by the CDC (kind gifts from Brandy Russel, Fort Collins, CO) and flavivirus envelop antibody (FE1), which cross-reacts with ZIKV, was purchased from Invitrogen (Cat. # MA1-71258). Two NB cell lines CRL-2266 and CRL-2267 were exposed to retinoic acid (RA) at 1 μM final concentration for 48 h (Breitman et al., 1980 (link)). Both cell lines exhibited partial differentiation as measured by morphologically and by immunostaining with anti-tubulin antibody.
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3

Culturing Neuroblastoma Cell Lines for ZIKV Study

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Five neuroblastoma (NB) cell lines were purchased from ATCC (New York, NY). CRL-2267, CCL-127, CRL-2271, CRL-2266, CRL- 2149, and CRL-2142, were cultured in Eagle’s Minimum Essential Media (EMEM) (ATCC, Manassas, VA) supplemented with 10% heat inactivated Fetal Bovine Serum (FBS), and L-Glutamine-penicillin-streptomycin solution (designated complete media) (Sigma, St. Louis, MO) at 37°C, 5% CO2. The stock cell cultures were grown in 25 mL or 75 mL flasks (Thermo-Scientific, Nunc, Rochester, NY). ZIKV strains KU501215 and MR 766 were provided by the CDC (kind gifts from Brandy Russel, Fort Collins, CO).
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