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uterine sarcoma cell lines mes sa  (ATCC)


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    ATCC uterine sarcoma cell lines mes sa
    Uterine Sarcoma Cell Lines Mes Sa, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 106 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/uterine+sarcoma+cell+lines+mes+sa/MES-SA/pm41146188-96-0-10
    Average 95 stars, based on 106 article reviews
    uterine sarcoma cell lines mes sa - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Modification:

    Article Title: Structure–Activity Relationships of 8-Hydroxyquinoline-Derived Mannich Bases with Tertiary Amines Targeting Multidrug-Resistant Cancer
    Article Snippet: .. The human uterine sarcoma cell lines MES-SA and the doxorubicin-selected MES-SA/Dx5 were obtained from ATCC (MES-SA: No. CRL-1976, MES-SA/Dx5: no. CRL-1977) and cultivated in Dulbecco’s modified Eagle’s medium (DMEM, Sigma-Aldrich, Hungary) supplemented with 10% fetal bovine serum, 5 mmol/L glutamine, and 50 unit/mL penicillin and streptomycin (Life Technologies, Hungary)., A431-ABCB1 cells were engineered by retroviral transduction, as described in. .. A431 cells were maintained in DMEM (Life Technologies) supplemented as above.

    Retroviral:

    Article Title: Structure–Activity Relationships of 8-Hydroxyquinoline-Derived Mannich Bases with Tertiary Amines Targeting Multidrug-Resistant Cancer
    Article Snippet: .. The human uterine sarcoma cell lines MES-SA and the doxorubicin-selected MES-SA/Dx5 were obtained from ATCC (MES-SA: No. CRL-1976, MES-SA/Dx5: no. CRL-1977) and cultivated in Dulbecco’s modified Eagle’s medium (DMEM, Sigma-Aldrich, Hungary) supplemented with 10% fetal bovine serum, 5 mmol/L glutamine, and 50 unit/mL penicillin and streptomycin (Life Technologies, Hungary)., A431-ABCB1 cells were engineered by retroviral transduction, as described in. .. A431 cells were maintained in DMEM (Life Technologies) supplemented as above.

    Transduction:

    Article Title: Structure–Activity Relationships of 8-Hydroxyquinoline-Derived Mannich Bases with Tertiary Amines Targeting Multidrug-Resistant Cancer
    Article Snippet: .. The human uterine sarcoma cell lines MES-SA and the doxorubicin-selected MES-SA/Dx5 were obtained from ATCC (MES-SA: No. CRL-1976, MES-SA/Dx5: no. CRL-1977) and cultivated in Dulbecco’s modified Eagle’s medium (DMEM, Sigma-Aldrich, Hungary) supplemented with 10% fetal bovine serum, 5 mmol/L glutamine, and 50 unit/mL penicillin and streptomycin (Life Technologies, Hungary)., A431-ABCB1 cells were engineered by retroviral transduction, as described in. .. A431 cells were maintained in DMEM (Life Technologies) supplemented as above.

    Cell Culture:

    Article Title: Safe delivery of a highly toxic anthracycline derivative through liposomal nanoformulation achieves complete cancer regression.
    Article Snippet: DLD-1 was purchased from ATCC and was maintained in RPMI. .. Uterine sarcoma cell lines Mes-Sa and Mes-Sa/Dx5 were purchased from ATCC and were cultured in DMEM. .. Pancreatic cell lines PANC-1 and Bx-PC-3, and lung cancer cell lines NCI-H1792 and LCLC were purchased from ATCC, and were kept in DMEM.

    Article Title: Complex formation and cytotoxicity of Triapine derivatives: a comparative solution study on the effect of the chalcogen atom and NH-methylation.
    Article Snippet: α-N-Heterocyclic thiosemicarbazones are an important class of investigational anticancer drugs.. The most prominent representative is 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (Triapine), which has shown promising results in clinical trials and is currently evaluated in phase III.. In this study, we investigated the influence of a chalcogen atom exchange from S (Triapine) to O (O-Triapine) and Se (SeTriapine) and the methylation of the hydrazonic NH moiety (Me-Triapine) on their complexation with Fe (II), Fe(III) and Cu(II) ions and their cytotoxicity.

    Article Title: Safe delivery of a highly toxic anthracycline derivative through liposomal nanoformulation achieves complete cancer regression
    Article Snippet: DLD-1 was purchased from ATCC and was maintained in RPMI. .. Uterine sarcoma cell lines Mes-Sa and Mes-Sa/Dx5 were purchased from ATCC and were cultured in DMEM. .. Pancreatic cell lines PANC-1 and Bx-PC-3, and lung cancer cell lines NCI-H1792 and LCLC were purchased from ATCC, and were kept in DMEM.

    MTT Assay:

    Article Title: Complex formation and cytotoxicity of Triapine derivatives: a comparative solution study on the effect of the chalcogen atom and NH-methylation.
    Article Snippet: α-N-Heterocyclic thiosemicarbazones are an important class of investigational anticancer drugs.. The most prominent representative is 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (Triapine), which has shown promising results in clinical trials and is currently evaluated in phase III.. In this study, we investigated the influence of a chalcogen atom exchange from S (Triapine) to O (O-Triapine) and Se (SeTriapine) and the methylation of the hydrazonic NH moiety (Me-Triapine) on their complexation with Fe (II), Fe(III) and Cu(II) ions and their cytotoxicity.

    Viability Assay:

    Article Title: Complex formation and cytotoxicity of Triapine derivatives: a comparative solution study on the effect of the chalcogen atom and NH-methylation.
    Article Snippet: α-N-Heterocyclic thiosemicarbazones are an important class of investigational anticancer drugs.. The most prominent representative is 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (Triapine), which has shown promising results in clinical trials and is currently evaluated in phase III.. In this study, we investigated the influence of a chalcogen atom exchange from S (Triapine) to O (O-Triapine) and Se (SeTriapine) and the methylation of the hydrazonic NH moiety (Me-Triapine) on their complexation with Fe (II), Fe(III) and Cu(II) ions and their cytotoxicity.



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    Image Search Results


    Effect of different collagen concentrations on the proliferative activity of BJ hTERT cells (cell counter) (ANOVA: F = 4.05, p = 0.02; *—difference from control, Dunnett’s test). The white boxplot represents the control against which the study groups were compared.

    Journal: Biomedicines

    Article Title: Development of a Collagen–Cerium Oxide Nanohydrogel for Wound Healing: In Vitro and In Vivo Evaluation

    doi: 10.3390/biomedicines13112623

    Figure Lengend Snippet: Effect of different collagen concentrations on the proliferative activity of BJ hTERT cells (cell counter) (ANOVA: F = 4.05, p = 0.02; *—difference from control, Dunnett’s test). The white boxplot represents the control against which the study groups were compared.

    Article Snippet: An initial series of experiments was conducted on the human fibroblast cell line BJ hTERT (American Type Culture Collection, ATCC, CRL-3627, Manassas, VA, USA; source: newborn foreskin) to determine the most effective and safe composition and concentrations of the developed nanodrug.

    Techniques: Activity Assay, Control

    Effect of different collagen concentrations on the metabolic activity of the BJ hTERT cell line in the MTT test (ANOVA OD: F = 51.49; p < 0.001; *— p < 0.001 compared with the control according to Dunnett’s test). The white boxplot represents the control against which the study groups were compared.

    Journal: Biomedicines

    Article Title: Development of a Collagen–Cerium Oxide Nanohydrogel for Wound Healing: In Vitro and In Vivo Evaluation

    doi: 10.3390/biomedicines13112623

    Figure Lengend Snippet: Effect of different collagen concentrations on the metabolic activity of the BJ hTERT cell line in the MTT test (ANOVA OD: F = 51.49; p < 0.001; *— p < 0.001 compared with the control according to Dunnett’s test). The white boxplot represents the control against which the study groups were compared.

    Article Snippet: An initial series of experiments was conducted on the human fibroblast cell line BJ hTERT (American Type Culture Collection, ATCC, CRL-3627, Manassas, VA, USA; source: newborn foreskin) to determine the most effective and safe composition and concentrations of the developed nanodrug.

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