normal mouse fibroblast cells l929 Search Results


99
ATCC l929 mouse fibroblasts
Cytotoxicity assay with <t>L929</t> mouse <t>fibroblasts</t> through ( a ) indirect contact (MTT protocol) ( n = 5) and ( b ) direct contact (20× amplification) of negative and positive controls and the scaffolds produced with PCL and: 1% wood cellulose (WC_1%); 2% wood cellulose (WC_2%); 1% corncob cellulose (CC_1%); 2% corncob cellulose (CC_2%). Scale bar: 100 μm. p < 0.001 (***).
L929 Mouse Fibroblasts, 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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97
Cell Signaling Technology Inc cell lines l929 fibroblasts
Cytotoxicity assay with <t>L929</t> mouse <t>fibroblasts</t> through ( a ) indirect contact (MTT protocol) ( n = 5) and ( b ) direct contact (20× amplification) of negative and positive controls and the scaffolds produced with PCL and: 1% wood cellulose (WC_1%); 2% wood cellulose (WC_2%); 1% corncob cellulose (CC_1%); 2% corncob cellulose (CC_2%). Scale bar: 100 μm. p < 0.001 (***).
Cell Lines L929 Fibroblasts, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Pasteur Institute l-929 mouse fibroblast cells
Cytotoxicity assay with <t>L929</t> mouse <t>fibroblasts</t> through ( a ) indirect contact (MTT protocol) ( n = 5) and ( b ) direct contact (20× amplification) of negative and positive controls and the scaffolds produced with PCL and: 1% wood cellulose (WC_1%); 2% wood cellulose (WC_2%); 1% corncob cellulose (CC_1%); 2% corncob cellulose (CC_2%). Scale bar: 100 μm. p < 0.001 (***).
L 929 Mouse Fibroblast Cells, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
JCRB Cell Bank l-929
Cytotoxicity assay with <t>L929</t> mouse <t>fibroblasts</t> through ( a ) indirect contact (MTT protocol) ( n = 5) and ( b ) direct contact (20× amplification) of negative and positive controls and the scaffolds produced with PCL and: 1% wood cellulose (WC_1%); 2% wood cellulose (WC_2%); 1% corncob cellulose (CC_1%); 2% corncob cellulose (CC_2%). Scale bar: 100 μm. p < 0.001 (***).
L 929, supplied by JCRB Cell Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
LGC Standards normal mouse fibroblasts l929
Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and <t>L929</t> cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).
Normal Mouse Fibroblasts L929, supplied by LGC Standards, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Millipore mouse fibroblast cells (l929
Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and <t>L929</t> cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).
Mouse Fibroblast Cells (L929, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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National Centre for Cell Science l929
Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and <t>L929</t> cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).
L929, supplied by National Centre for Cell Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Seikagaku corporation anti-ifn-β
Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and <t>L929</t> cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).
Anti Ifn β, supplied by Seikagaku corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC mouse areolar connective tissue l929 cells
Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and <t>L929</t> cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).
Mouse Areolar Connective Tissue L929 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
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90
Helmholtz Zentrum fur Infektionsforschung GmbH cd40l-expressing l929 cells
Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and <t>L929</t> cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).
Cd40l Expressing L929 Cells, supplied by Helmholtz Zentrum fur Infektionsforschung GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
DSMZ l 929 mouse fibroblasts
Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and <t>L929</t> cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).
L 929 Mouse Fibroblasts, supplied by DSMZ, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Cytotoxicity assay with L929 mouse fibroblasts through ( a ) indirect contact (MTT protocol) ( n = 5) and ( b ) direct contact (20× amplification) of negative and positive controls and the scaffolds produced with PCL and: 1% wood cellulose (WC_1%); 2% wood cellulose (WC_2%); 1% corncob cellulose (CC_1%); 2% corncob cellulose (CC_2%). Scale bar: 100 μm. p < 0.001 (***).

Journal: Journal of Functional Biomaterials

Article Title: Corncob Cellulose Scaffolds: A New Sustainable Temporary Implant for Cartilage Replacement

doi: 10.3390/jfb13020063

Figure Lengend Snippet: Cytotoxicity assay with L929 mouse fibroblasts through ( a ) indirect contact (MTT protocol) ( n = 5) and ( b ) direct contact (20× amplification) of negative and positive controls and the scaffolds produced with PCL and: 1% wood cellulose (WC_1%); 2% wood cellulose (WC_2%); 1% corncob cellulose (CC_1%); 2% corncob cellulose (CC_2%). Scale bar: 100 μm. p < 0.001 (***).

Article Snippet: The biocompatibility of the manufactured scaffolds was assessed using L929 mouse fibroblasts (ATCC number CCL-1) and following the ISO 10993-5 and ISO 10993-12 guidelines [ ].

Techniques: Cytotoxicity Assay, Amplification, Produced

Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and L929 cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).

Journal: Molecules

Article Title: The Antioxidant, Cytotoxic and Antimicrobial Potential of Phenolic Acids-Enriched Extract of Elicited Hairy Roots of Salvia bulleyana

doi: 10.3390/molecules27030992

Figure Lengend Snippet: Cytotoxic effect of S. bulleyana extract towards the LoVo, AGS, HeLa and L929 cell lines. The cell viability was calculated for four experiments, including three replicates for each compound. Complete RMPI-1640 medium (cRPMI) was used as a positive control of cell viability (100% viable cells) and 0.03% H 2 O 2 as a negative control of cell viability (5% for LoVo, 2.2% for AGS, 3.2% for HeLa, 3.3% for L929). *—determination of statistical significance for untreated cells vs. cells treated with tested plant extract for the same cell line according to the Kruskal–Wallis test ( p < 0.05).

Article Snippet: In vitro cytotoxicity testing was performed using human HeLa (CCL-2, American Type Culture Collection (ATCC), Rockville, MD, USA) cervix adenocarcinoma epithelial cells, human AGS (CRL-1739, ATCC, Rockville, MD, USA) gastric adenocarcinoma epithelial cells, human colon epithelial LoVo (CCL-229™, ATCC, Rockville, MD, USA) and normal mouse fibroblasts L929 (LGC Standards, Middlesex, UK).

Techniques: Positive Control, Negative Control