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Search results for the GEO ID: GSE17714
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GSM389810
GPL570
GI-LI-N_hypoxia neuroblastoma cell line under hypoxic conditions cell line: GI-LI-N condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389811
GPL570
GI-LI-N_normoxia neuroblastoma cell line under normoxic conditions cell line: GI-LI-N condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM389812
GPL570
ACN_hypoxia neuroblastoma cell line under hypoxic conditions cell line: ACN condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389813
GPL570
ACN_normoxia neuroblastoma cell line under normoxic conditions cell line: ACN condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM389814
GPL570
SHEP-2_hypoxia neuroblastoma cell line under hypoxic conditions cell line: SHEP-2 condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389815
GPL570
SHEP-2_normoxia neuroblastoma cell line under normoxic conditions cell line: SHEP-2 condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM389816
GPL570
SK-N-BE2(C)_hypoxia neuroblastoma cell line under hypoxic conditions cell line: SK-N-BE2(C) condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389817
GPL570
SK-N-BE2(C)_normoxia neuroblastoma cell line under normoxic conditions cell line: SK-N-BE2(C) condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM389818
GPL570
IMR-32_hypoxia neuroblastoma cell line under hypoxic conditions cell line: IMR-32 condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389819
GPL570
IMR-32_normoxia neuroblastoma cell line under normoxic conditions cell line: IMR-32 condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM389820
GPL570
SK-N-F1_hypoxia neuroblastoma cell line under hypoxic conditions cell line: SK-N-F1 condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389822
GPL570
SK-N-F1_normoxia neuroblastoma cell line under normoxic conditions cell line: SK-N-F1 condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM389823
GPL570
LAN-1_hypoxia neuroblastoma cell line under hypoxic conditions cell line: LAN-1 condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389824
GPL570
LAN-1_normoxia neuroblastoma cell line under normoxic conditions cell line: LAN-1 condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM389825
GPL570
SK-N-SH_hypoxia neuroblastoma cell line under hypoxic conditions cell line: SK-N-SH condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389827
GPL570
SK-N-SH_normoxia neuroblastoma cell line under normoxic conditions cell line: SK-N-SH condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM389828
GPL570
GI-ME-N_hypoxia neuroblastoma cell line under hypoxic conditions cell line: GI-ME-N condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM389829
GPL570
GI-ME-N_normoxia neuroblastoma cell line under normoxic conditions cell line: GI-ME-N condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd), at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM442195
GPL570
SHEP21N_normoxia neuroblastoma cell line under normoxic conditions cell line: SHEP21N mycn: without overexpression condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, 100 ug/mL streptomycin (Euroclone Ltd), and 50 ng/mL tetracycline (Sigma, St. Louis, MO)at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM442197
GPL570
SHEP21N_hypoxia neuroblastoma cell line under hypoxic conditions cell line: SHEP21N mycn: without overexpression condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, 100 ug/mL streptomycin (Euroclone Ltd), and 50 ng/mL tetracycline (Sigma, St. Louis, MO)at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
GSM442198
GPL570
SHEP21N_MYC_normoxia neuroblastoma cell line under normoxic conditions cell line: SHEP21N mycn: with overexpression condition: normoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd) at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2.
GSM442199
GPL570
SHEP21N_MYC_hypoxia neuroblastoma cell line under hypoxic conditions cell line: SHEP21N mycn: with overexpression condition: hypoxia The cell lines were cultured in RPMI 16140 (Euroclone Ltd., Celbio, Milan, Italy), supplemented with 10% heat-inactivated fetal bovine serum (Sigma, Milan Italy), 2 mmol/L L-glutamine, 10 mM Hepes, 100 units/mL penicillin, and 100 ug/mL streptomycin (Euroclone Ltd) at 37° C in a humidified incubator containing 20% O2, 5% CO2, and 75% N2. Hypoxic conditions (1% O2) were achieved by culturing the cells in an anaerobic workstation incubator (BUG BOX, Jouan, ALC International S.r.l., Cologno Monzese, Milano, Italy) flushed with a gas mixture containing 1% O2, 5% CO2, and balanced N2 at 37°C in a humidified atmosphere. Oxygen tension in the medium was measured with a portable, trace oxygen analyzer (Oxi 315i/set, WTW; VWR International, Milano, Italy).
 
 
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