human gbm cell line u 87 mg (ATCC)
Structured Review

Human Gbm Cell Line U 87 Mg, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 10512 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/u+87+mg+cell+lines/U-87+MG/pmc13156593-197-2-8
Average 99 stars, based on 10512 article reviews
Images
1) Product Images from "AAV transduction of human glioblastoma cell lines induces perturbation in cell proliferation"
Article Title: AAV transduction of human glioblastoma cell lines induces perturbation in cell proliferation
Journal: Molecular Therapy Oncology
doi: 10.1016/j.omton.2026.201216
Figure Legend Snippet: Differential transduction of human GBM cell lines with AAV vector serotypes (A) Representative images of U-87 MG and patient-derived cell lines transduced with AAV1, 2, 1/2, 6, and 6.2 expressing eGFP and pBS control-treated control. Green, GFP expression; magenta, EdU staining; blue, Hoechst staining. Scale bars, 100 μm. (B) Quantitation of the transduction efficiency for all serotypes in each cell line as determined by GFP expression. All data presented as mean (SD), n = 3 biological replicates.
Techniques Used: Transduction, Plasmid Preparation, Derivative Assay, Expressing, Control, Staining, Quantitation Assay
Figure Legend Snippet: AAV transduced CD44-positive cell populations with greater efficiency (A) Transduction efficiency of AAV1, 2, 1/2, 6, and 6.2 in CD44-positive and -negative cell populations. Two-way ANOVA showed no significant interaction between the effects of AAV serotype and CD44 expression on transduction efficiency in all cell lines. There was a significant main effect of CD44 expression in U-87 MG ( p = 0.007), case 1 ( p = 0.0003), and case 4 ( p = 0.010) but no statistical significance was found following Sidak’s multiple comparisons test. (B) CD44 expression in human GBM cell lines following AAV treatment. (C) Proliferation of the CD44-positive cell population normalized to values from NTC-treated control. Treatments were compared against their respective pBS-treated control. All data presented as mean (SD), n = 3 biological replicates. Statistical significance is shown as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
Techniques Used: Transduction, Expressing, Control
Figure Legend Snippet: Reductions in cell number and proliferation following AAV treatment persisted in the absence of transgene expression (A) Representative images of U-87 MG, cases 2 and 5 transduced with AAV expressing eGFP or no transgene, along with their respective pBS controls. Green, GFP expression; magenta, EdU staining; blue, Hoechst staining. Scale bars, 100 μm. (B) Total cell number and (C) cell proliferation in the 24 h prior to fixation, normalized to values from NTC-treated control. Treatments were compared against their respective pBS-treated control. All data presented as mean (SD), n = 3 biological replicates. Statistical significance is shown as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.
Techniques Used: Expressing, Transduction, Staining, Control
Figure Legend Snippet: AAV treatment induced cell-cycle arrest at G1 in cases 2 and 5 but not U-87 MG (A) Cumulative cytotoxicity was evaluated by LDH release assay 4 days following AAV treatment, normalized to the maximal LDH release from the Triton X-100 control. No statistical significance was detected. (B) Percentage of cells in each cell cycle phase (G0/G1, S, and G2/M) were quantified via DNA content profiling (see also ). All data presented as mean (SD), n = 3 biological replicates. Treatments were compared against their respective pBS-treated control. Statistical significance is shown as G0/G1 phases: ∗∗∗∗ p < 0.0001; S phase: † p < 0.05; G2/M phases: # p < 0.05, ### p < 0.001.
Techniques Used: Lactate Dehydrogenase Assay, Control
Related Articles
Cell Culture:Article Title: In Vitro Sonodynamic Therapy Using a High Throughput 3D Glioblastoma Spheroid Model with 5-ALA and TMZ Sonosensitizers. Article Snippet: 5-Aminolevulinic acid hydrochloride (99% purity, molecular weight 167.59 g mol−1, A16942-ME) Temozolomide (98%, molecular weight 194.15 g mol−1, T2577-25MG), Invitrogen Cell ROX Green reagent (C10444), Trypan Blue (0.4%, Thermofisher Scientific, USA), Invitrogen ready probes cell viability imaging kit, Blue/Green (R37609), GLPBIO Cell Counting Kit-8 (CCK-8), Promega CellTiter-Glo (R) 3D cell viability assay (G9681), Gibco DPBS (14 040 133), Gibco DMEM (11 995 040), are purchased from Fisher Scientific, USA, and Dimethyl Sulfoxide (for molecular biology, D8418), Millipore Sigma, USA. .. Modification:Article Title: In Vitro Sonodynamic Therapy Using a High Throughput 3D Glioblastoma Spheroid Model with 5-ALA and TMZ Sonosensitizers. Article Snippet: 5-Aminolevulinic acid hydrochloride (99% purity, molecular weight 167.59 g mol−1, A16942-ME) Temozolomide (98%, molecular weight 194.15 g mol−1, T2577-25MG), Invitrogen Cell ROX Green reagent (C10444), Trypan Blue (0.4%, Thermofisher Scientific, USA), Invitrogen ready probes cell viability imaging kit, Blue/Green (R37609), GLPBIO Cell Counting Kit-8 (CCK-8), Promega CellTiter-Glo (R) 3D cell viability assay (G9681), Gibco DPBS (14 040 133), Gibco DMEM (11 995 040), are purchased from Fisher Scientific, USA, and Dimethyl Sulfoxide (for molecular biology, D8418), Millipore Sigma, USA. .. other:Article Title: Preclinical and dose-ranging assessment of hESC-derived dopaminergic progenitors for a clinical trial on Parkinson's disease. Article Snippet: Retrovirus presence was tested using Reverse Transcriptase Assay (Roche, Basel, Switzerland). Article Title: Protocol for mass spectrometric profiling of lysine malonylation by lysine acetyltransferase in CRISPRi K562 cell lines. Article Snippet: Generate dCas9-KRAB (or dCas9-KARB-MeCP2)-expressing K562 cell line in house according to Gilbert et al.3 Note: Ours were a gift from the Jonathan Weissman Lab. At the time of preparation of this protocol, dCas9-KRAB-expressing HEK-293, MCF7, and Article Title: Protocol for mass spectrometric profiling of lysine malonylation by lysine acetyltransferase in CRISPRi K562 cell lines Article Snippet: Note: Ours were a gift from the Jonathan Weissman Lab. At the time of preparation of this protocol, dCas9-KRAB-expressing HEK-293, MCF7, and |
