41965039 endothelial cell growth medium 2 promocell cat Search Results


96
PromoCell endothelial growth medium 2
Endothelial Growth Medium 2, supplied by PromoCell, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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iXCells Biotechnologies endothelial cell growth medium 2
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ATCC endothelial cell medium 2
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PromoCell endothelial cell growth medium 2
Endothelial Cell Growth Medium 2, supplied by PromoCell, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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endothelial cell growth medium 2 - by Bioz Stars, 2026-10
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PromoCell microvascular endothelial growth medium 2
Microvascular Endothelial Growth Medium 2, supplied by PromoCell, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Merck & Co huvec
Schematic representation of the antioxidant activity of pomegranate leaf extract and derived metabolites in single <t>and</t> <t>co-cultured</t> cell lines. Primary antioxidant activity was evaluated by simultaneously incubating the pomegranate leaf extract (TE) and derived metabolites (EA and LU) with the pro-oxidant agent H 2 O 2 for 5 h. LU in HDF and EA in <t>HUVEC</t> resulted in a significant decrease in ROS-mediated cytotoxicity, thereby acting as primary antioxidants. Secondary antioxidant activity was evaluated by exposing the pre-incubating cells with pomegranate leaf extract (TE) and derived metabolites (EA and LU) for 24 h, followed by exposure to the pro-oxidant agent H 2 O 2 for 5 h. TE in the HDF-HUVEC resulted in a significant decrease in the ROS-mediated cytotoxicity, along with a significant increase in the mRNA expression of genes involved in the Nrf2 pathway, thereby acting as a secondary antioxidant.
Huvec, supplied by Merck & Co, 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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Innopharmascreen Inc huvecs
Schematic representation of the antioxidant activity of pomegranate leaf extract and derived metabolites in single <t>and</t> <t>co-cultured</t> cell lines. Primary antioxidant activity was evaluated by simultaneously incubating the pomegranate leaf extract (TE) and derived metabolites (EA and LU) with the pro-oxidant agent H 2 O 2 for 5 h. LU in HDF and EA in <t>HUVEC</t> resulted in a significant decrease in ROS-mediated cytotoxicity, thereby acting as primary antioxidants. Secondary antioxidant activity was evaluated by exposing the pre-incubating cells with pomegranate leaf extract (TE) and derived metabolites (EA and LU) for 24 h, followed by exposure to the pro-oxidant agent H 2 O 2 for 5 h. TE in the HDF-HUVEC resulted in a significant decrease in the ROS-mediated cytotoxicity, along with a significant increase in the mRNA expression of genes involved in the Nrf2 pathway, thereby acting as a secondary antioxidant.
Huvecs, supplied by Innopharmascreen Inc, 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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Becton Dickinson huvecs
Schematic representation of the antioxidant activity of pomegranate leaf extract and derived metabolites in single <t>and</t> <t>co-cultured</t> cell lines. Primary antioxidant activity was evaluated by simultaneously incubating the pomegranate leaf extract (TE) and derived metabolites (EA and LU) with the pro-oxidant agent H 2 O 2 for 5 h. LU in HDF and EA in <t>HUVEC</t> resulted in a significant decrease in ROS-mediated cytotoxicity, thereby acting as primary antioxidants. Secondary antioxidant activity was evaluated by exposing the pre-incubating cells with pomegranate leaf extract (TE) and derived metabolites (EA and LU) for 24 h, followed by exposure to the pro-oxidant agent H 2 O 2 for 5 h. TE in the HDF-HUVEC resulted in a significant decrease in the ROS-mediated cytotoxicity, along with a significant increase in the mRNA expression of genes involved in the Nrf2 pathway, thereby acting as a secondary antioxidant.
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Biochrom penicillin/streptomycin (ps)
Schematic representation of the antioxidant activity of pomegranate leaf extract and derived metabolites in single <t>and</t> <t>co-cultured</t> cell lines. Primary antioxidant activity was evaluated by simultaneously incubating the pomegranate leaf extract (TE) and derived metabolites (EA and LU) with the pro-oxidant agent H 2 O 2 for 5 h. LU in HDF and EA in <t>HUVEC</t> resulted in a significant decrease in ROS-mediated cytotoxicity, thereby acting as primary antioxidants. Secondary antioxidant activity was evaluated by exposing the pre-incubating cells with pomegranate leaf extract (TE) and derived metabolites (EA and LU) for 24 h, followed by exposure to the pro-oxidant agent H 2 O 2 for 5 h. TE in the HDF-HUVEC resulted in a significant decrease in the ROS-mediated cytotoxicity, along with a significant increase in the mRNA expression of genes involved in the Nrf2 pathway, thereby acting as a secondary antioxidant.
Penicillin/Streptomycin (Ps), supplied by Biochrom, 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
Corning Life Sciences 1% collagen
Schematic representation of the antioxidant activity of pomegranate leaf extract and derived metabolites in single <t>and</t> <t>co-cultured</t> cell lines. Primary antioxidant activity was evaluated by simultaneously incubating the pomegranate leaf extract (TE) and derived metabolites (EA and LU) with the pro-oxidant agent H 2 O 2 for 5 h. LU in HDF and EA in <t>HUVEC</t> resulted in a significant decrease in ROS-mediated cytotoxicity, thereby acting as primary antioxidants. Secondary antioxidant activity was evaluated by exposing the pre-incubating cells with pomegranate leaf extract (TE) and derived metabolites (EA and LU) for 24 h, followed by exposure to the pro-oxidant agent H 2 O 2 for 5 h. TE in the HDF-HUVEC resulted in a significant decrease in the ROS-mediated cytotoxicity, along with a significant increase in the mRNA expression of genes involved in the Nrf2 pathway, thereby acting as a secondary antioxidant.
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Schematic representation of the antioxidant activity of pomegranate leaf extract and derived metabolites in single and co-cultured cell lines. Primary antioxidant activity was evaluated by simultaneously incubating the pomegranate leaf extract (TE) and derived metabolites (EA and LU) with the pro-oxidant agent H 2 O 2 for 5 h. LU in HDF and EA in HUVEC resulted in a significant decrease in ROS-mediated cytotoxicity, thereby acting as primary antioxidants. Secondary antioxidant activity was evaluated by exposing the pre-incubating cells with pomegranate leaf extract (TE) and derived metabolites (EA and LU) for 24 h, followed by exposure to the pro-oxidant agent H 2 O 2 for 5 h. TE in the HDF-HUVEC resulted in a significant decrease in the ROS-mediated cytotoxicity, along with a significant increase in the mRNA expression of genes involved in the Nrf2 pathway, thereby acting as a secondary antioxidant.

Journal: Scientific Reports

Article Title: Comparative antioxidant activity of pomegranate leaf extract and derived metabolites in single and co-cultured cell lines

doi: 10.1038/s41598-025-20130-6

Figure Lengend Snippet: Schematic representation of the antioxidant activity of pomegranate leaf extract and derived metabolites in single and co-cultured cell lines. Primary antioxidant activity was evaluated by simultaneously incubating the pomegranate leaf extract (TE) and derived metabolites (EA and LU) with the pro-oxidant agent H 2 O 2 for 5 h. LU in HDF and EA in HUVEC resulted in a significant decrease in ROS-mediated cytotoxicity, thereby acting as primary antioxidants. Secondary antioxidant activity was evaluated by exposing the pre-incubating cells with pomegranate leaf extract (TE) and derived metabolites (EA and LU) for 24 h, followed by exposure to the pro-oxidant agent H 2 O 2 for 5 h. TE in the HDF-HUVEC resulted in a significant decrease in the ROS-mediated cytotoxicity, along with a significant increase in the mRNA expression of genes involved in the Nrf2 pathway, thereby acting as a secondary antioxidant.

Article Snippet: The human umbilical endothelial, HUVEC, cell line (C122-03, Merck), was cultured in the Endothelial Cell Growth Medium 2 (ECGM2, PromoCell, Italy) supplemented with the Supplement Mix (PromoCell) according to manufacturer’s instruction.

Techniques: Antioxidant Activity Assay, Derivative Assay, Cell Culture, Expressing