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Sarstedt pore size polyester transwell inserts
Pore Size Polyester Transwell Inserts, supplied by Sarstedt, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pore+size+polyester+transwell+inserts/inserts+transwell/10__3390_slash_ijms27083683-195-18-24
Average 86 stars, based on 1 article reviews
pore size polyester transwell inserts - by Bioz Stars, 2026-09
86/100 stars

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Pore Size:

Article Title: Analysis of Phosphate Transporters in Peritoneal Cells and Tissues and Their Transport Kinetics In Vitro
Article Snippet: .. Polarized monolayers of mesothelial or endothelial cells were established by seeding 5 × 10 4 cells onto 0.4 μm pore size polyester Transwell inserts (24-well; SARSTEDT AG & Co. KG, Nümbrecht, Germany). ..

Article Title: Analysis of Phosphate Transporters in Peritoneal Cells and Tissues and Their Transport Kinetics In Vitro
Article Snippet: .. Polarized monolayers of mesothelial or endothelial cells were established by seeding 5 × 104 cells onto 0.4 μm pore size polyester Transwell inserts (24-well; SARSTEDT AG & Co. KG, Nümbrecht, Germany). ..



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Effects of fungal extracts on the TEER (A, B, C) and fluorescein permeability (D) of HCE-T cells. (A, B, C) HCE-T cells were cultured on a <t>translucent</t> membrane of a <t>transwell</t> insert for 72 h and treated with mushroom extracts. The TEER was measured every 24 h. (D) After TEER measurement, cells were washed and exposed to fluorescein for 2 h to determine permeability. BAC was used as a positive control. Data were normalised to 4% FCS and presented as mean ± standard deviation. n = 3; *p < 0.05, **p < 0.01, ***p < 0.001.
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SPL Life Sciences transwell polyester (pet) filter inserts with a membrane pore size of 3 μm
Effects of fungal extracts on the TEER (A, B, C) and fluorescein permeability (D) of HCE-T cells. (A, B, C) HCE-T cells were cultured on a <t>translucent</t> membrane of a <t>transwell</t> insert for 72 h and treated with mushroom extracts. The TEER was measured every 24 h. (D) After TEER measurement, cells were washed and exposed to fluorescein for 2 h to determine permeability. BAC was used as a positive control. Data were normalised to 4% FCS and presented as mean ± standard deviation. n = 3; *p < 0.05, **p < 0.01, ***p < 0.001.
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Effects of fungal extracts on the TEER (A, B, C) and fluorescein permeability (D) of HCE-T cells. (A, B, C) HCE-T cells were cultured on a translucent membrane of a transwell insert for 72 h and treated with mushroom extracts. The TEER was measured every 24 h. (D) After TEER measurement, cells were washed and exposed to fluorescein for 2 h to determine permeability. BAC was used as a positive control. Data were normalised to 4% FCS and presented as mean ± standard deviation. n = 3; *p < 0.05, **p < 0.01, ***p < 0.001.

Journal: Frontiers in Pharmacology

Article Title: Evaluation of in vitro pharmacological activities of medicinal mushrooms in the context of dry eye disease

doi: 10.3389/fphar.2025.1557359

Figure Lengend Snippet: Effects of fungal extracts on the TEER (A, B, C) and fluorescein permeability (D) of HCE-T cells. (A, B, C) HCE-T cells were cultured on a translucent membrane of a transwell insert for 72 h and treated with mushroom extracts. The TEER was measured every 24 h. (D) After TEER measurement, cells were washed and exposed to fluorescein for 2 h to determine permeability. BAC was used as a positive control. Data were normalised to 4% FCS and presented as mean ± standard deviation. n = 3; *p < 0.05, **p < 0.01, ***p < 0.001.

Article Snippet: HCE-T cells (3 × 10 4 cells) were inoculated with 400 μL of culture medium onto a translucent polyester (PET) membrane transwell insert (0.4 μm pore size; Greiner bio-one), and 1 mL of culture medium was added into the basolateral chamber.

Techniques: Permeability, Cell Culture, Membrane, Positive Control, Standard Deviation