human neuroblastoma nb cell lines Search Results


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JCRB Cell Bank human neuroblastoma cell line tgw-sre-luc, clone 42, jcrb0618
Human Neuroblastoma Cell Line Tgw Sre Luc, Clone 42, Jcrb0618, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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CNS Research human neuroblastoma cell line sh-sy5y
Human Neuroblastoma Cell Line Sh Sy5y, supplied by CNS Research, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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INFINIUM Inc human neuroblastoma cell lines sk-n-sh
Animal and cellular studies.
Human Neuroblastoma Cell Lines Sk N Sh, supplied by INFINIUM Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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JCRB Cell Bank human neuroblastoma cell line sh-sy5y
Animal and cellular studies.
Human Neuroblastoma Cell Line Sh Sy5y, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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JCRB Cell Bank human neuroblastoma cell line kp-n-si9s
Animal and cellular studies.
Human Neuroblastoma Cell Line Kp N Si9s, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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AbbVie Inc bb10 clonal isolate of the sima human neuroblastoma cell line
Animal and cellular studies.
Bb10 Clonal Isolate Of The Sima Human Neuroblastoma Cell Line, supplied by AbbVie Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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JIAHE INTERNATIONAL CO LTD human neuroblastoma cell line sh-sy5y cell line
( A,B ) The p11 protein levels were measured using western blots. The p11 protein levels were normalized against GAPDH. The results demonstrated that IFN-α treatment down-regulated the p11 protein levels in <t>SH-sy5y</t> cells. ( A ) Different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 24 h produced significant dose-dependent decreases in the p11 protein levels. ( B ) Time-dependent (0, 6, 12, 24, 36, and 48 h) effects in IFN-α (1000 IU/mL) treated cells, with reduced p11 protein levels at 24 h and the lowest levels at 36 h. ( C ) Dose-dependent effect of IFN-α on the p11 mRNA levels in SH-sy5y cells, which were normalized against GAPDH. SH-sy5y cells were treated with hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 16 h, and p11 mRNA levels were measured using real-time PCR. The real-time PCR results demonstrated no effects of hINF-α-2b on the p11 mRNA levels. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.
Human Neuroblastoma Cell Line Sh Sy5y Cell Line, supplied by JIAHE INTERNATIONAL CO LTD, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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BioTherapeutics Inc human neuroblastoma cell lines sk-n-sh, sk-n-as and sh-sy5y
( A,B ) The p11 protein levels were measured using western blots. The p11 protein levels were normalized against GAPDH. The results demonstrated that IFN-α treatment down-regulated the p11 protein levels in <t>SH-sy5y</t> cells. ( A ) Different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 24 h produced significant dose-dependent decreases in the p11 protein levels. ( B ) Time-dependent (0, 6, 12, 24, 36, and 48 h) effects in IFN-α (1000 IU/mL) treated cells, with reduced p11 protein levels at 24 h and the lowest levels at 36 h. ( C ) Dose-dependent effect of IFN-α on the p11 mRNA levels in SH-sy5y cells, which were normalized against GAPDH. SH-sy5y cells were treated with hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 16 h, and p11 mRNA levels were measured using real-time PCR. The real-time PCR results demonstrated no effects of hINF-α-2b on the p11 mRNA levels. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.
Human Neuroblastoma Cell Lines Sk N Sh, Sk N As And Sh Sy5y, supplied by BioTherapeutics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Welgene inc human neuroblastoma cell line sh-sy5y
( A,B ) The p11 protein levels were measured using western blots. The p11 protein levels were normalized against GAPDH. The results demonstrated that IFN-α treatment down-regulated the p11 protein levels in <t>SH-sy5y</t> cells. ( A ) Different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 24 h produced significant dose-dependent decreases in the p11 protein levels. ( B ) Time-dependent (0, 6, 12, 24, 36, and 48 h) effects in IFN-α (1000 IU/mL) treated cells, with reduced p11 protein levels at 24 h and the lowest levels at 36 h. ( C ) Dose-dependent effect of IFN-α on the p11 mRNA levels in SH-sy5y cells, which were normalized against GAPDH. SH-sy5y cells were treated with hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 16 h, and p11 mRNA levels were measured using real-time PCR. The real-time PCR results demonstrated no effects of hINF-α-2b on the p11 mRNA levels. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.
Human Neuroblastoma Cell Line Sh Sy5y, supplied by Welgene inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+neuroblastoma+nb+cell+lines/human+neuroblastoma+cell+line+sh+sy5y/pmc11809180-82-4-9
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BioWhittaker Molecular Applications human neuroblastoma sk-n-be cell line
( A,B ) The p11 protein levels were measured using western blots. The p11 protein levels were normalized against GAPDH. The results demonstrated that IFN-α treatment down-regulated the p11 protein levels in <t>SH-sy5y</t> cells. ( A ) Different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 24 h produced significant dose-dependent decreases in the p11 protein levels. ( B ) Time-dependent (0, 6, 12, 24, 36, and 48 h) effects in IFN-α (1000 IU/mL) treated cells, with reduced p11 protein levels at 24 h and the lowest levels at 36 h. ( C ) Dose-dependent effect of IFN-α on the p11 mRNA levels in SH-sy5y cells, which were normalized against GAPDH. SH-sy5y cells were treated with hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 16 h, and p11 mRNA levels were measured using real-time PCR. The real-time PCR results demonstrated no effects of hINF-α-2b on the p11 mRNA levels. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.
Human Neuroblastoma Sk N Be Cell Line, supplied by BioWhittaker Molecular Applications, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Shengxing International Development Co Ltd human neuroblastoma cell lines sh-sy5y
( A,B ) The p11 protein levels were measured using western blots. The p11 protein levels were normalized against GAPDH. The results demonstrated that IFN-α treatment down-regulated the p11 protein levels in <t>SH-sy5y</t> cells. ( A ) Different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 24 h produced significant dose-dependent decreases in the p11 protein levels. ( B ) Time-dependent (0, 6, 12, 24, 36, and 48 h) effects in IFN-α (1000 IU/mL) treated cells, with reduced p11 protein levels at 24 h and the lowest levels at 36 h. ( C ) Dose-dependent effect of IFN-α on the p11 mRNA levels in SH-sy5y cells, which were normalized against GAPDH. SH-sy5y cells were treated with hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 16 h, and p11 mRNA levels were measured using real-time PCR. The real-time PCR results demonstrated no effects of hINF-α-2b on the p11 mRNA levels. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.
Human Neuroblastoma Cell Lines Sh Sy5y, supplied by Shengxing International Development Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+neuroblastoma+nb+cell+lines/human+neuroblastoma+cell+lines+sh+sy5y/10__1039_slash_c7ra00485k-107-1-9
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SuperArray Bioscience Corporation human sk-n-mc neuroblastoma cell line
Evaluation by gene expression profiling of the molecular targets of curcumin in cancer cells.
Human Sk N Mc Neuroblastoma Cell Line, supplied by SuperArray Bioscience Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Animal and cellular studies.

Journal: International Journal of Molecular Sciences

Article Title: DNA Methylation as a Biomarker of Treatment Response Variability in Serious Mental Illnesses: A Systematic Review Focused on Bipolar Disorder, Schizophrenia, and Major Depressive Disorder

doi: 10.3390/ijms19103026

Figure Lengend Snippet: Animal and cellular studies.

Article Snippet: Human neuroblastoma cell lines SK-N-SH , Infinium HumanMethylation27 BeadChip + bisulfite sequencing , • Quetiapine decreases DNA methylation of the CpG3 island of SLC6A4 , [ ] .

Techniques: High Performance Liquid Chromatography, Polymerase Chain Reaction, Sequencing, Methylated DNA Immunoprecipitation, Methylation, Real-time Polymerase Chain Reaction, Methylation Sequencing, DNA Methylation Assay, Cell Culture

( A,B ) The p11 protein levels were measured using western blots. The p11 protein levels were normalized against GAPDH. The results demonstrated that IFN-α treatment down-regulated the p11 protein levels in SH-sy5y cells. ( A ) Different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 24 h produced significant dose-dependent decreases in the p11 protein levels. ( B ) Time-dependent (0, 6, 12, 24, 36, and 48 h) effects in IFN-α (1000 IU/mL) treated cells, with reduced p11 protein levels at 24 h and the lowest levels at 36 h. ( C ) Dose-dependent effect of IFN-α on the p11 mRNA levels in SH-sy5y cells, which were normalized against GAPDH. SH-sy5y cells were treated with hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 16 h, and p11 mRNA levels were measured using real-time PCR. The real-time PCR results demonstrated no effects of hINF-α-2b on the p11 mRNA levels. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.

Journal: Scientific Reports

Article Title: Probable involvement of p11 with interferon alpha induced depression

doi: 10.1038/srep17029

Figure Lengend Snippet: ( A,B ) The p11 protein levels were measured using western blots. The p11 protein levels were normalized against GAPDH. The results demonstrated that IFN-α treatment down-regulated the p11 protein levels in SH-sy5y cells. ( A ) Different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 24 h produced significant dose-dependent decreases in the p11 protein levels. ( B ) Time-dependent (0, 6, 12, 24, 36, and 48 h) effects in IFN-α (1000 IU/mL) treated cells, with reduced p11 protein levels at 24 h and the lowest levels at 36 h. ( C ) Dose-dependent effect of IFN-α on the p11 mRNA levels in SH-sy5y cells, which were normalized against GAPDH. SH-sy5y cells were treated with hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL) for 16 h, and p11 mRNA levels were measured using real-time PCR. The real-time PCR results demonstrated no effects of hINF-α-2b on the p11 mRNA levels. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.

Article Snippet: Human neuroblastoma cell line (SH-sy5y cell line, Jiahe Biotech Company, Shanghai, China) was cultured in Dulbecco’s modified Eagle medium (DMEM) containing 10% fetal bovine serum, 50 U/mL penicillin, and 50 mg/mL streptomycin at 37 °C, with 5% CO 2 .

Techniques: Western Blot, Produced, Real-time Polymerase Chain Reaction

( A–C ) IFN-α treatment down-regulated the 5-HTR1b and 5-HTR4 protein levels in a dose-dependent manner. The 5-HTR1b and 5-HTR4 protein levels were determined using western blotting. Cells were treated with different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL; 0 IU/mL as the control) for 24 h. ( A ) The western blots detected a significant dose-dependent decrease in the 5-HTR1b/4 protein levels after hIFN-α-2b treatment. The 5-HTR1b (B) and 5-HTR4 ( C ) protein levels were normalized against GAPDH. ( D,E ) The real-time PCR results show that IFN-α treatment has no influence on the 5-HTR1b/4 mRNA levels in SH-sy5y cells. Cells were treated with different doses of hIFN-α-2b for 16 h. The values were normalized against GAPDH. ( D ) The 5-HTR1b mRNA levels in hIFN-α-2b treatment groups had no significant difference compared with the controls ( P > 0.05). ( E ) The 5-HTR4 mRNA levels in hIFN-α-2b treatment groups had no significant difference compared with the controls ( P > 0.05). All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.

Journal: Scientific Reports

Article Title: Probable involvement of p11 with interferon alpha induced depression

doi: 10.1038/srep17029

Figure Lengend Snippet: ( A–C ) IFN-α treatment down-regulated the 5-HTR1b and 5-HTR4 protein levels in a dose-dependent manner. The 5-HTR1b and 5-HTR4 protein levels were determined using western blotting. Cells were treated with different doses of hIFN-α-2b (0, 50, 500, 1000, 2000, and 3000 IU/mL; 0 IU/mL as the control) for 24 h. ( A ) The western blots detected a significant dose-dependent decrease in the 5-HTR1b/4 protein levels after hIFN-α-2b treatment. The 5-HTR1b (B) and 5-HTR4 ( C ) protein levels were normalized against GAPDH. ( D,E ) The real-time PCR results show that IFN-α treatment has no influence on the 5-HTR1b/4 mRNA levels in SH-sy5y cells. Cells were treated with different doses of hIFN-α-2b for 16 h. The values were normalized against GAPDH. ( D ) The 5-HTR1b mRNA levels in hIFN-α-2b treatment groups had no significant difference compared with the controls ( P > 0.05). ( E ) The 5-HTR4 mRNA levels in hIFN-α-2b treatment groups had no significant difference compared with the controls ( P > 0.05). All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.

Article Snippet: Human neuroblastoma cell line (SH-sy5y cell line, Jiahe Biotech Company, Shanghai, China) was cultured in Dulbecco’s modified Eagle medium (DMEM) containing 10% fetal bovine serum, 50 U/mL penicillin, and 50 mg/mL streptomycin at 37 °C, with 5% CO 2 .

Techniques: Western Blot, Control, Real-time Polymerase Chain Reaction

( A ) Western blots showed the 5-HTR1b and 5-HTR4 protein levels in SH-sy5y cells treated with hIFN-α-2b (1000 IU/mL) at various time points (0, 6, 12, 24, 36, and 48 h). ( B,C ) The 5-HTR1b and 5-HTR4 protein levels were normalized against GAPDH. The results showed that the 5-HTR1b ( B ) and 5-HTR4 ( C ) levels declined at 6 h and reached their lowest levels at 24 h. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.

Journal: Scientific Reports

Article Title: Probable involvement of p11 with interferon alpha induced depression

doi: 10.1038/srep17029

Figure Lengend Snippet: ( A ) Western blots showed the 5-HTR1b and 5-HTR4 protein levels in SH-sy5y cells treated with hIFN-α-2b (1000 IU/mL) at various time points (0, 6, 12, 24, 36, and 48 h). ( B,C ) The 5-HTR1b and 5-HTR4 protein levels were normalized against GAPDH. The results showed that the 5-HTR1b ( B ) and 5-HTR4 ( C ) levels declined at 6 h and reached their lowest levels at 24 h. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05 and ** P < 0.01.

Article Snippet: Human neuroblastoma cell line (SH-sy5y cell line, Jiahe Biotech Company, Shanghai, China) was cultured in Dulbecco’s modified Eagle medium (DMEM) containing 10% fetal bovine serum, 50 U/mL penicillin, and 50 mg/mL streptomycin at 37 °C, with 5% CO 2 .

Techniques: Western Blot

( A ) SH-sy5y cells were treated with 1000 IU/mL hIFNα-2b, and with an equal volume of PBS as the control. The proteins in cytomembrane of SH-sy5y cells were extracted at 24 h. The p11, 5-HTR1b and 5-HTR4 protein levels were analyzed using western blotting. ( B ) The levels of p11, 5-HTR1b and 5-HTR4 protein in cytomembrane were normalized against Pan-cadherin. Tublin test was performed to eliminate the contamination from cytoplasm to cytomembrane proteins. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. ** P < 0.01.

Journal: Scientific Reports

Article Title: Probable involvement of p11 with interferon alpha induced depression

doi: 10.1038/srep17029

Figure Lengend Snippet: ( A ) SH-sy5y cells were treated with 1000 IU/mL hIFNα-2b, and with an equal volume of PBS as the control. The proteins in cytomembrane of SH-sy5y cells were extracted at 24 h. The p11, 5-HTR1b and 5-HTR4 protein levels were analyzed using western blotting. ( B ) The levels of p11, 5-HTR1b and 5-HTR4 protein in cytomembrane were normalized against Pan-cadherin. Tublin test was performed to eliminate the contamination from cytoplasm to cytomembrane proteins. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. ** P < 0.01.

Article Snippet: Human neuroblastoma cell line (SH-sy5y cell line, Jiahe Biotech Company, Shanghai, China) was cultured in Dulbecco’s modified Eagle medium (DMEM) containing 10% fetal bovine serum, 50 U/mL penicillin, and 50 mg/mL streptomycin at 37 °C, with 5% CO 2 .

Techniques: Control, Western Blot

After plasmid transfection for 24 h, 1000 U/mL hIFNα-2b or PBS was added to the medium. Total proteins were extracted at 48 h. and the p11, 5-HTR1b and 5-HTR4 protein levels were analyzed using western blotting. Total RNA was extracted at 36 h and reverse transcription was applied to produce cDNA. The 5-HTR1b and 5-HTR4 mRNA levels were analyzed using real-time PCR. ( A ) SH-sy5y cells were transfected with p11-pcDNA3.0 containing full-length p11cDNA, with pcDNA3.0 as the control. ( B–D ) The p11 ( B ), 5-HTR1b ( C ), and 5-HTR4 ( D ) protein levels in p11-pcDNA3.0 transfection groups were normalized against GAPDH. ( E ) After PBS treatment, SH-sy5y cells were transfected with p11-miRNA that interfered with the expression of p11, miRNA-control vector as the control. ( F–H ) The p11 ( F ), 5-HTR1b ( G ), and 5-HTR4 ( H ) protein levels in p11-miRNA transfection groups were normalized against GAPDH. ( I,J ) mRNA levels of 5-HTR1b ( I ) and 5-HTR4 ( J ) in SH-sy5y cells in each transfection group was analyzed using real-time PCR and normalized against GAPDH. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05, ** P < 0.01 and NS , no significant difference.

Journal: Scientific Reports

Article Title: Probable involvement of p11 with interferon alpha induced depression

doi: 10.1038/srep17029

Figure Lengend Snippet: After plasmid transfection for 24 h, 1000 U/mL hIFNα-2b or PBS was added to the medium. Total proteins were extracted at 48 h. and the p11, 5-HTR1b and 5-HTR4 protein levels were analyzed using western blotting. Total RNA was extracted at 36 h and reverse transcription was applied to produce cDNA. The 5-HTR1b and 5-HTR4 mRNA levels were analyzed using real-time PCR. ( A ) SH-sy5y cells were transfected with p11-pcDNA3.0 containing full-length p11cDNA, with pcDNA3.0 as the control. ( B–D ) The p11 ( B ), 5-HTR1b ( C ), and 5-HTR4 ( D ) protein levels in p11-pcDNA3.0 transfection groups were normalized against GAPDH. ( E ) After PBS treatment, SH-sy5y cells were transfected with p11-miRNA that interfered with the expression of p11, miRNA-control vector as the control. ( F–H ) The p11 ( F ), 5-HTR1b ( G ), and 5-HTR4 ( H ) protein levels in p11-miRNA transfection groups were normalized against GAPDH. ( I,J ) mRNA levels of 5-HTR1b ( I ) and 5-HTR4 ( J ) in SH-sy5y cells in each transfection group was analyzed using real-time PCR and normalized against GAPDH. All results were representative of three separate experiments. The data represented the mean ± S.E. compared with the controls. * P < 0.05, ** P < 0.01 and NS , no significant difference.

Article Snippet: Human neuroblastoma cell line (SH-sy5y cell line, Jiahe Biotech Company, Shanghai, China) was cultured in Dulbecco’s modified Eagle medium (DMEM) containing 10% fetal bovine serum, 50 U/mL penicillin, and 50 mg/mL streptomycin at 37 °C, with 5% CO 2 .

Techniques: Plasmid Preparation, Transfection, Western Blot, Reverse Transcription, Real-time Polymerase Chain Reaction, Control, Expressing

Evaluation by gene expression profiling of the molecular targets of curcumin in cancer cells.

Journal: Toxins

Article Title: Curcumin―The Paradigm of a Multi-Target Natural Compound with Applications in Cancer Prevention and Treatment

doi: 10.3390/toxins2010128

Figure Lengend Snippet: Evaluation by gene expression profiling of the molecular targets of curcumin in cancer cells.

Article Snippet: Superarray , human SK-N-MC neuroblastoma cell line , Curcumin is a potent radiosensitizer that inhibits growth of human neuroblastoma cells and downregulates radiation-induced pro-survival factors implicating NF-kB transcription factor. , [ ] .

Techniques: Gene Expression, Expressing, Activity Assay, Knock-Out, Ubiquitin Proteomics, Quantitative Proteomics, Control, Derivative Assay