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u 87 mg cell lines  (ATCC)
99
ATCC u 87 mg cell lines
Hypoxia impacts gene expression and signaling pathways in GBM cells (A) Hypoxia-responsive pathways were identified using Partek Flow software under double filter MI50 and fold change >+1.5 criteria. (B) Expression of candidate genes in PBT030 cells following 48-h hypoxia exposure compared to cells under normoxic conditions. (C) Expression of candidate genes <t>in</t> <t>U-87</t> MG cells after 48 h of hypoxia compared to cells maintained under normoxic conditions. Representative bar graphs are derived from at least two independent experiments, with 28S used as the reference gene for all experiments.
U 87 Mg Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
u 87 mg cell lines - by Bioz Stars, 2026-05
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u 87mg human glioblastoma cells  (ATCC)
99
ATCC u 87mg human glioblastoma cells
Hypoxia impacts gene expression and signaling pathways in GBM cells (A) Hypoxia-responsive pathways were identified using Partek Flow software under double filter MI50 and fold change >+1.5 criteria. (B) Expression of candidate genes in PBT030 cells following 48-h hypoxia exposure compared to cells under normoxic conditions. (C) Expression of candidate genes <t>in</t> <t>U-87</t> MG cells after 48 h of hypoxia compared to cells maintained under normoxic conditions. Representative bar graphs are derived from at least two independent experiments, with 28S used as the reference gene for all experiments.
U 87mg Human Glioblastoma Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/u 87mg human glioblastoma cells/product/ATCC
Average 99 stars, based on 1 article reviews
u 87mg human glioblastoma cells - by Bioz Stars, 2026-05
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u87 mg cells  (ATCC)
99
ATCC u87 mg cells
Hypoxia impacts gene expression and signaling pathways in GBM cells (A) Hypoxia-responsive pathways were identified using Partek Flow software under double filter MI50 and fold change >+1.5 criteria. (B) Expression of candidate genes in PBT030 cells following 48-h hypoxia exposure compared to cells under normoxic conditions. (C) Expression of candidate genes <t>in</t> <t>U-87</t> MG cells after 48 h of hypoxia compared to cells maintained under normoxic conditions. Representative bar graphs are derived from at least two independent experiments, with 28S used as the reference gene for all experiments.
U87 Mg Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/u87 mg cells/product/ATCC
Average 99 stars, based on 1 article reviews
u87 mg cells - by Bioz Stars, 2026-05
99/100 stars
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u87 mg atcc version  (ATCC)
99
ATCC u87 mg atcc version
Hypoxia impacts gene expression and signaling pathways in GBM cells (A) Hypoxia-responsive pathways were identified using Partek Flow software under double filter MI50 and fold change >+1.5 criteria. (B) Expression of candidate genes in PBT030 cells following 48-h hypoxia exposure compared to cells under normoxic conditions. (C) Expression of candidate genes <t>in</t> <t>U-87</t> MG cells after 48 h of hypoxia compared to cells maintained under normoxic conditions. Representative bar graphs are derived from at least two independent experiments, with 28S used as the reference gene for all experiments.
U87 Mg Atcc Version, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/u87 mg atcc version/product/ATCC
Average 99 stars, based on 1 article reviews
u87 mg atcc version - by Bioz Stars, 2026-05
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u87mg  (ATCC)
99
ATCC u87mg
Cells expressing IGF-1R ( A and E ), SH-SY5Y ( B and F ), <t>U87MG</t> ( C and G ), and rat primary neuronal culture ( D and H ) were stimulated with 10 nM ligands for 20 min. Phosphorylation of Akt (A to D) and Erk1/2 (E to H) was assessed by Western blot. Data were normalized to GAPDH loading control and are shown relative to IGF-1–induced signal. Identical GAPDH loading controls are shown for the figure pairs (A) and (E), (B) and (F), and (D) and (H) because the samples in each pair were run on the same gel. Representative blots are shown and all blots are shown in the Supplementary Materials. Color coding as in . Asterisks indicate significance versus IGF-1 [(A), (B), and (E)] or versus control [(C), (D), (F), (G), and (H)]. (* P < 0.05; ** P < 0.01; *** P < 0.001; # P < 0.0001; ns, not significant according to ANOVA). X indicates that this sample was not included in the study.
U87mg, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/u87mg/product/ATCC
Average 99 stars, based on 1 article reviews
u87mg - by Bioz Stars, 2026-05
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u 87 mg  (ATCC)
99
ATCC u 87 mg
Cells expressing IGF-1R ( A and E ), SH-SY5Y ( B and F ), <t>U87MG</t> ( C and G ), and rat primary neuronal culture ( D and H ) were stimulated with 10 nM ligands for 20 min. Phosphorylation of Akt (A to D) and Erk1/2 (E to H) was assessed by Western blot. Data were normalized to GAPDH loading control and are shown relative to IGF-1–induced signal. Identical GAPDH loading controls are shown for the figure pairs (A) and (E), (B) and (F), and (D) and (H) because the samples in each pair were run on the same gel. Representative blots are shown and all blots are shown in the Supplementary Materials. Color coding as in . Asterisks indicate significance versus IGF-1 [(A), (B), and (E)] or versus control [(C), (D), (F), (G), and (H)]. (* P < 0.05; ** P < 0.01; *** P < 0.001; # P < 0.0001; ns, not significant according to ANOVA). X indicates that this sample was not included in the study.
U 87 Mg, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/u 87 mg/product/ATCC
Average 99 stars, based on 1 article reviews
u 87 mg - by Bioz Stars, 2026-05
99/100 stars
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human u87 mg glioblastoma cells  (ATCC)
99
ATCC human u87 mg glioblastoma cells
Cells expressing IGF-1R ( A and E ), SH-SY5Y ( B and F ), <t>U87MG</t> ( C and G ), and rat primary neuronal culture ( D and H ) were stimulated with 10 nM ligands for 20 min. Phosphorylation of Akt (A to D) and Erk1/2 (E to H) was assessed by Western blot. Data were normalized to GAPDH loading control and are shown relative to IGF-1–induced signal. Identical GAPDH loading controls are shown for the figure pairs (A) and (E), (B) and (F), and (D) and (H) because the samples in each pair were run on the same gel. Representative blots are shown and all blots are shown in the Supplementary Materials. Color coding as in . Asterisks indicate significance versus IGF-1 [(A), (B), and (E)] or versus control [(C), (D), (F), (G), and (H)]. (* P < 0.05; ** P < 0.01; *** P < 0.001; # P < 0.0001; ns, not significant according to ANOVA). X indicates that this sample was not included in the study.
Human U87 Mg Glioblastoma Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human u87 mg glioblastoma cells/product/ATCC
Average 99 stars, based on 1 article reviews
human u87 mg glioblastoma cells - by Bioz Stars, 2026-05
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Hypoxia impacts gene expression and signaling pathways in GBM cells (A) Hypoxia-responsive pathways were identified using Partek Flow software under double filter MI50 and fold change >+1.5 criteria. (B) Expression of candidate genes in PBT030 cells following 48-h hypoxia exposure compared to cells under normoxic conditions. (C) Expression of candidate genes in U-87 MG cells after 48 h of hypoxia compared to cells maintained under normoxic conditions. Representative bar graphs are derived from at least two independent experiments, with 28S used as the reference gene for all experiments.

Journal: Molecular Therapy Oncology

Article Title: CBX6 and CA9 as predictive indicators and therapeutic targets in GBM

doi: 10.1016/j.omton.2026.201159

Figure Lengend Snippet: Hypoxia impacts gene expression and signaling pathways in GBM cells (A) Hypoxia-responsive pathways were identified using Partek Flow software under double filter MI50 and fold change >+1.5 criteria. (B) Expression of candidate genes in PBT030 cells following 48-h hypoxia exposure compared to cells under normoxic conditions. (C) Expression of candidate genes in U-87 MG cells after 48 h of hypoxia compared to cells maintained under normoxic conditions. Representative bar graphs are derived from at least two independent experiments, with 28S used as the reference gene for all experiments.

Article Snippet: U-251 MG and U-87 MG cell lines were purchased from the American Type Culture Collection (ATCC).

Techniques: Gene Expression, Protein-Protein interactions, Software, Expressing, Derivative Assay

Cells expressing IGF-1R ( A and E ), SH-SY5Y ( B and F ), U87MG ( C and G ), and rat primary neuronal culture ( D and H ) were stimulated with 10 nM ligands for 20 min. Phosphorylation of Akt (A to D) and Erk1/2 (E to H) was assessed by Western blot. Data were normalized to GAPDH loading control and are shown relative to IGF-1–induced signal. Identical GAPDH loading controls are shown for the figure pairs (A) and (E), (B) and (F), and (D) and (H) because the samples in each pair were run on the same gel. Representative blots are shown and all blots are shown in the Supplementary Materials. Color coding as in . Asterisks indicate significance versus IGF-1 [(A), (B), and (E)] or versus control [(C), (D), (F), (G), and (H)]. (* P < 0.05; ** P < 0.01; *** P < 0.001; # P < 0.0001; ns, not significant according to ANOVA). X indicates that this sample was not included in the study.

Journal: Science Advances

Article Title: An engineered insulin analog with dual insulin and IGF-1 receptor agonism and distinct signaling

doi: 10.1126/sciadv.aeb7558

Figure Lengend Snippet: Cells expressing IGF-1R ( A and E ), SH-SY5Y ( B and F ), U87MG ( C and G ), and rat primary neuronal culture ( D and H ) were stimulated with 10 nM ligands for 20 min. Phosphorylation of Akt (A to D) and Erk1/2 (E to H) was assessed by Western blot. Data were normalized to GAPDH loading control and are shown relative to IGF-1–induced signal. Identical GAPDH loading controls are shown for the figure pairs (A) and (E), (B) and (F), and (D) and (H) because the samples in each pair were run on the same gel. Representative blots are shown and all blots are shown in the Supplementary Materials. Color coding as in . Asterisks indicate significance versus IGF-1 [(A), (B), and (E)] or versus control [(C), (D), (F), (G), and (H)]. (* P < 0.05; ** P < 0.01; *** P < 0.001; # P < 0.0001; ns, not significant according to ANOVA). X indicates that this sample was not included in the study.

Article Snippet: The U87MG (ATCC, HTB-14) glioblastoma cell line was grown in minimum essential medium supplemented with 10% FBS, 1% streptomycin-penicillin, and 2 mM l -glutamine.

Techniques: Expressing, Phospho-proteomics, Western Blot, Control