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u87 fluc  (ATCC)


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    ATCC u87 fluc
    U87 Fluc, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 44 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/u87+fluc/U-87+MG-Luc2/pmc11609628-39-12-13
    Average 94 stars, based on 44 article reviews
    u87 fluc - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Multiple Displacement Amplification:

    Article Title: An Innovative Mitochondrial-targeted Gene Therapy for Cancer Treatment
    Article Snippet: The human TNBC cell lines MDA-MB-231 (GenTarget, San Diego, CA), MDA-MB-468 (GenTarget) and BT-20 (ATCC), and GBM cell lines U251 (MilliporeSigma, Burlington, MA), drug-resistant U251-TMZ (in-house developed), U87 and GL261 (Creative Bioarray, Shirley, NY) were used for in vitro cytotoxicity, surface binding, AAV gene delivery, gene expression, or mechanism studies. .. The MDA-MB-231-FLuc (GenTarget), 4T1-FLuc (ATCC), U87, U251, and U87-FLuc (ATCC) were used to develop xenograft mouse models (immunocompromised and immunocompetent) for evaluating the in vivo anti-tumor efficacy of mLumiOpto. .. All cell culture media, supplements and other reagents were purchased from Gibco unless otherwise specified.

    In Vivo:

    Article Title: An Innovative Mitochondrial-targeted Gene Therapy for Cancer Treatment
    Article Snippet: The human TNBC cell lines MDA-MB-231 (GenTarget, San Diego, CA), MDA-MB-468 (GenTarget) and BT-20 (ATCC), and GBM cell lines U251 (MilliporeSigma, Burlington, MA), drug-resistant U251-TMZ (in-house developed), U87 and GL261 (Creative Bioarray, Shirley, NY) were used for in vitro cytotoxicity, surface binding, AAV gene delivery, gene expression, or mechanism studies. .. The MDA-MB-231-FLuc (GenTarget), 4T1-FLuc (ATCC), U87, U251, and U87-FLuc (ATCC) were used to develop xenograft mouse models (immunocompromised and immunocompetent) for evaluating the in vivo anti-tumor efficacy of mLumiOpto. .. All cell culture media, supplements and other reagents were purchased from Gibco unless otherwise specified.



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    Image Search Results


    IncuCyte S3 live cell system (4×) Live spheroids images analysis shows the proliferation curves of the confluence ratio of U87 single spheroid upon using the protocol steps. The first triplicate failed to convert the aggregates to spheroids without using the washing solution. However, following the protocol showed consistent reproducibility for the single spheroids on three triplicates 2, 3, and 4. The images show the difference between the shape of the aggregates and the successful shape of the spheroid.

    Journal: bioRxiv

    Article Title: Swift Formation of Optimal Single Spheroids towards In-Vitro 3-Dimensional Tumour Models

    doi: 10.1101/2021.12.16.472941

    Figure Lengend Snippet: IncuCyte S3 live cell system (4×) Live spheroids images analysis shows the proliferation curves of the confluence ratio of U87 single spheroid upon using the protocol steps. The first triplicate failed to convert the aggregates to spheroids without using the washing solution. However, following the protocol showed consistent reproducibility for the single spheroids on three triplicates 2, 3, and 4. The images show the difference between the shape of the aggregates and the successful shape of the spheroid.

    Article Snippet: The human glioblastoma U87 MG-Red-FLuc (Bioware Brite, PerkinElmer, Waltham, Massachusetts, USA) was the authorized cell line in all experiments.

    Techniques:

    IncuCyte S3 live cell system (4×) Live spheroids images analysis shows (A) the proliferation curves of the confluence ratio of U87 single spheroid for four spheroids shrinked to the half size after 24 hours then grew over time. The images show the negative effect of using different type of plate. (B) the image shows the instant adherence of the cells when using different plate without washing. (C) The image shows the cells gathered when the anti-adherence solution. However, the plate material was not suitable to allow the tightness of the cells. A crack in the middle appeared after the centrifugation directly.

    Journal: bioRxiv

    Article Title: Swift Formation of Optimal Single Spheroids towards In-Vitro 3-Dimensional Tumour Models

    doi: 10.1101/2021.12.16.472941

    Figure Lengend Snippet: IncuCyte S3 live cell system (4×) Live spheroids images analysis shows (A) the proliferation curves of the confluence ratio of U87 single spheroid for four spheroids shrinked to the half size after 24 hours then grew over time. The images show the negative effect of using different type of plate. (B) the image shows the instant adherence of the cells when using different plate without washing. (C) The image shows the cells gathered when the anti-adherence solution. However, the plate material was not suitable to allow the tightness of the cells. A crack in the middle appeared after the centrifugation directly.

    Article Snippet: The human glioblastoma U87 MG-Red-FLuc (Bioware Brite, PerkinElmer, Waltham, Massachusetts, USA) was the authorized cell line in all experiments.

    Techniques: Centrifugation

    Cell tightness and interaction analysis of U87 MG spheroids. H & E stain of spheroid slices from (A) the core area, and (B) top rim area of 7 days spheroid generated from 400 cells.

    Journal: bioRxiv

    Article Title: Swift Formation of Optimal Single Spheroids towards In-Vitro 3-Dimensional Tumour Models

    doi: 10.1101/2021.12.16.472941

    Figure Lengend Snippet: Cell tightness and interaction analysis of U87 MG spheroids. H & E stain of spheroid slices from (A) the core area, and (B) top rim area of 7 days spheroid generated from 400 cells.

    Article Snippet: The human glioblastoma U87 MG-Red-FLuc (Bioware Brite, PerkinElmer, Waltham, Massachusetts, USA) was the authorized cell line in all experiments.

    Techniques: Staining, Generated

    IncuCyte S3 live cell system (4×) Live spheroids images show the potential of using the protocol to obtain single spheroids from various cell lines. The comparison shows consistency in the mean size and similar standard deviation for 6 individual samples from each cell line (U87 MG, SF188, SEBTA-027 human brain tumours, DU145 prostate human tumour, and TRAMP-C1 prostate murine tumour). The scale bar is 400 µm.

    Journal: bioRxiv

    Article Title: Swift Formation of Optimal Single Spheroids towards In-Vitro 3-Dimensional Tumour Models

    doi: 10.1101/2021.12.16.472941

    Figure Lengend Snippet: IncuCyte S3 live cell system (4×) Live spheroids images show the potential of using the protocol to obtain single spheroids from various cell lines. The comparison shows consistency in the mean size and similar standard deviation for 6 individual samples from each cell line (U87 MG, SF188, SEBTA-027 human brain tumours, DU145 prostate human tumour, and TRAMP-C1 prostate murine tumour). The scale bar is 400 µm.

    Article Snippet: The human glioblastoma U87 MG-Red-FLuc (Bioware Brite, PerkinElmer, Waltham, Massachusetts, USA) was the authorized cell line in all experiments.

    Techniques: Comparison, Standard Deviation

    Expression of (A) E-cadherin and Beta Actin. (B) Vinculin and vimentin in U87MG cells grown either in a monolayer, or as spheroids derived from 400 cells for 24 hours and 10 days.

    Journal: bioRxiv

    Article Title: Swift Formation of Optimal Single Spheroids towards In-Vitro 3-Dimensional Tumour Models

    doi: 10.1101/2021.12.16.472941

    Figure Lengend Snippet: Expression of (A) E-cadherin and Beta Actin. (B) Vinculin and vimentin in U87MG cells grown either in a monolayer, or as spheroids derived from 400 cells for 24 hours and 10 days.

    Article Snippet: The human glioblastoma U87 MG-Red-FLuc (Bioware Brite, PerkinElmer, Waltham, Massachusetts, USA) was the authorized cell line in all experiments.

    Techniques: Expressing, Derivative Assay

    Morphological growth and luciferase activity in U87MG cells. Representative images of U87MG cells at 3 (A) , 36 (B) , and 72 (C) hours at 20x magnification after taking out of Cryofrizide. A luciferase receptor gene was used to tag the U87MG cells. Steady growth and attenuation of the morphological pattern of U87MG cells present at 36 and 72 h. (D) Detection of luciferase activity expressed in luciferase units (LFU) in U87MG and hRPE cells. Results are the average of three independent experiments.

    Journal: Frontiers in Pharmacology

    Article Title: Combined Therapy With Avastin, a PAF Receptor Antagonist and a Lipid Mediator Inhibited Glioblastoma Tumor Growth

    doi: 10.3389/fphar.2021.746470

    Figure Lengend Snippet: Morphological growth and luciferase activity in U87MG cells. Representative images of U87MG cells at 3 (A) , 36 (B) , and 72 (C) hours at 20x magnification after taking out of Cryofrizide. A luciferase receptor gene was used to tag the U87MG cells. Steady growth and attenuation of the morphological pattern of U87MG cells present at 36 and 72 h. (D) Detection of luciferase activity expressed in luciferase units (LFU) in U87MG and hRPE cells. Results are the average of three independent experiments.

    Article Snippet: The human cell line U87 MG-Red-Flug (U87MG) containing a luciferase-expressing gene was purchased from PerkinElmer (Waltham, MA).

    Techniques: Luciferase, Activity Assay

    (A) Experimental design, showing bregma level and site of tumor cell implantation in anesthetized athymic nude female mice, secured in a stereotactic head frame. (B) Timeline showing GBM implantation, imaging, and treatments. Mice underwent stereotactic implantation of the luciferase-modified U87MG cells on day 0 and were monitored during a 30-day survival period. Treatment was started on day 13 post-implantation. In vivo bioluminescent imaging was performed on days 13, 20, and 30 post-implantation. On day 30, mice were sacrificed, and ex vivo MRI was conducted on perfused brains.

    Journal: Frontiers in Pharmacology

    Article Title: Combined Therapy With Avastin, a PAF Receptor Antagonist and a Lipid Mediator Inhibited Glioblastoma Tumor Growth

    doi: 10.3389/fphar.2021.746470

    Figure Lengend Snippet: (A) Experimental design, showing bregma level and site of tumor cell implantation in anesthetized athymic nude female mice, secured in a stereotactic head frame. (B) Timeline showing GBM implantation, imaging, and treatments. Mice underwent stereotactic implantation of the luciferase-modified U87MG cells on day 0 and were monitored during a 30-day survival period. Treatment was started on day 13 post-implantation. In vivo bioluminescent imaging was performed on days 13, 20, and 30 post-implantation. On day 30, mice were sacrificed, and ex vivo MRI was conducted on perfused brains.

    Article Snippet: The human cell line U87 MG-Red-Flug (U87MG) containing a luciferase-expressing gene was purchased from PerkinElmer (Waltham, MA).

    Techniques: Imaging, Luciferase, Modification, In Vivo, Ex Vivo

    Quantification of bioluminescent signals from tumors. Radiance (Radiance × 10 6 ) values from regions of interest in mice from all groups were averaged and compared on days 13, 20, and 30 following intracranial implantation of U87-Luc cells. Tumor-bearing mice treated with (A) LAU-0901, Avastin, LAU-0901 + Avastin and (B) ELV, ELV + LAU-0901, and ELV + Avastin were observed have significantly reduced tumorigenesis when compared to vehicle-treated mice. All values are mean ± SEM ( n = 5–7), * p < 0.05.

    Journal: Frontiers in Pharmacology

    Article Title: Combined Therapy With Avastin, a PAF Receptor Antagonist and a Lipid Mediator Inhibited Glioblastoma Tumor Growth

    doi: 10.3389/fphar.2021.746470

    Figure Lengend Snippet: Quantification of bioluminescent signals from tumors. Radiance (Radiance × 10 6 ) values from regions of interest in mice from all groups were averaged and compared on days 13, 20, and 30 following intracranial implantation of U87-Luc cells. Tumor-bearing mice treated with (A) LAU-0901, Avastin, LAU-0901 + Avastin and (B) ELV, ELV + LAU-0901, and ELV + Avastin were observed have significantly reduced tumorigenesis when compared to vehicle-treated mice. All values are mean ± SEM ( n = 5–7), * p < 0.05.

    Article Snippet: The human cell line U87 MG-Red-Flug (U87MG) containing a luciferase-expressing gene was purchased from PerkinElmer (Waltham, MA).

    Techniques: