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normal mouse l929 fibroblast cell line  (ATCC)


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    ATCC normal mouse l929 fibroblast cell line
    Normal Mouse L929 Fibroblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 958 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/normal+mouse+l929+fibroblast+cell+line/HCT+116%3B+Colon+Carcinoma%3B+Human/pm40733198-204-9-22
    Average 97 stars, based on 958 article reviews
    normal mouse l929 fibroblast cell line - by Bioz Stars, 2026-10
    97/100 stars

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    Activity Assay:

    Article Title: Chemical Composition, Cytotoxicity, and Encapsulation of Lavender Essential Oil ( Lavandula angustifolia ) in Alginate Hydrogel—Application and Therapeutic Effect on Animal Model
    Article Snippet: .. The biological activity of LEO was analyzed using a normal mouse L929 fibroblast cell line (L cell, L-929, derivative of strain L, ATCC ® CCL-1TM). .. Cells were seeded into 96-well plates (TPP, Techno Plastic Products AG, Trasadingen, Switzerland) at a density of 3.5 × 10 3 per well (for CCK-8, LDH, and NRU assays) and into 12-well plates at 4 × 10 4 per well (for morphological analysis) and were maintained under standard culture conditions (37 °C, 5% CO 2 , 95% relative humidity) prior to experimental treatment.

    Article Title: Chemical Composition, Cytotoxicity, and Encapsulation of Lavender Essential Oil ( Lavandula angustifolia ) in Alginate Hydrogel-Application and Therapeutic Effect on Animal Model.
    Article Snippet: .. The biological activity of LEO was analyzed using a normal mouse L929 fibroblast cell line (L cell, L-929, derivative of strain L, ATCC® CCL-1TM). .. Cells were seeded into 96-well plates (TPP, Techno Plastic Products AG, Trasadingen, Switzerland) at a density of 3.5 × 103 per well (for CCK-8, LDH, and NRU assays) and into 12-well plates at 4 × 104 per well (for morphological analysis) and were maintained under standard culture conditions (37 ◦C, 5% CO2, 95% relative humidity) prior to experimental treatment.



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    Effect of royal jelly (RJ) on normal cells. <t>L929</t> and PBMC were used as models of normal cells. The MTT assay indicated that RJ has no cytotoxic effect on L929 and PBMC cells (A). Analysis of apoptosis using Annexin-V/PI staining and flow cytometry revealed that RJ has no significant apoptotic effect on normal cells (B). Hemolytic activity evolution suggested that the hemolysis rate decreases when RJ concentration increases (C). The values are given as the mean SD of three independent experiments. * P ≤0.05 represents significant statistical changes from the control sample
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    Effect of royal jelly (RJ) on normal cells. L929 and PBMC were used as models of normal cells. The MTT assay indicated that RJ has no cytotoxic effect on L929 and PBMC cells (A). Analysis of apoptosis using Annexin-V/PI staining and flow cytometry revealed that RJ has no significant apoptotic effect on normal cells (B). Hemolytic activity evolution suggested that the hemolysis rate decreases when RJ concentration increases (C). The values are given as the mean SD of three independent experiments. * P ≤0.05 represents significant statistical changes from the control sample

    Journal: Iranian Journal of Basic Medical Sciences

    Article Title: Royal jelly induces ROS-mediated apoptosis in acute lymphoblastic leukemia (ALL)-derived Nalm-6 cells: Shedding light on novel therapeutic approaches for ALL

    doi: 10.22038/IJBMS.2024.76261.16498

    Figure Lengend Snippet: Effect of royal jelly (RJ) on normal cells. L929 and PBMC were used as models of normal cells. The MTT assay indicated that RJ has no cytotoxic effect on L929 and PBMC cells (A). Analysis of apoptosis using Annexin-V/PI staining and flow cytometry revealed that RJ has no significant apoptotic effect on normal cells (B). Hemolytic activity evolution suggested that the hemolysis rate decreases when RJ concentration increases (C). The values are given as the mean SD of three independent experiments. * P ≤0.05 represents significant statistical changes from the control sample

    Article Snippet: Cell culture and treatment Acute Lymphoblastic Leukemia cell line (Nalm-6) and normal mouse fibroblast cell line (L929) were purchased from the Pasteur Institute collection (Tehran, Iran).

    Techniques: MTT Assay, Staining, Flow Cytometry, Activity Assay, Concentration Assay, Control