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2-compartment boyden chamber with a physical barrier of an 8 μm polycarbonate membrane transwell insert  (Corning Life Sciences)

 
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    Structured Review

    Corning Life Sciences 2-compartment boyden chamber with a physical barrier of an 8 μm polycarbonate membrane transwell insert
    2 Compartment Boyden Chamber With A Physical Barrier Of An 8 μm Polycarbonate Membrane Transwell Insert, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/compartment+insert/2+compartment+boyden+chamber+with+a+physical+barrier+of+an+8+%CE%BCm+polycarbonate+membrane+transwell+insert/10__3390_slash_ijms26051822-302-6-21
    Average 90 stars, based on 1 article reviews
    2-compartment boyden chamber with a physical barrier of an 8 μm polycarbonate membrane transwell insert - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Activity Assay:

    Article Title: Comparison of gene expression and biotransformation activity of HepaRG cells under static and dynamic culture conditions
    Article Snippet: .. For static culture conditions, cells were seeded in black coated 96-well plates (Greiner Bio-One, Frickenhausen, Germany; 9000 cells per well in 100 μL) for CYP activity under baseline conditions; in transparent 24-well plates (Greiner Bio-One; 55,000 cells per well in 500 μL) for RNA isolation and CYP induction studies; or in Transwell inserts (Corning; 25,000 cells per insert in 250 μL in the apical compartment (750 μL in the basolateral compartment); 0.4 μm pore 12 mm polyester membrane) for immunocytochemistry. ..

    Isolation:

    Article Title: Comparison of gene expression and biotransformation activity of HepaRG cells under static and dynamic culture conditions
    Article Snippet: .. For static culture conditions, cells were seeded in black coated 96-well plates (Greiner Bio-One, Frickenhausen, Germany; 9000 cells per well in 100 μL) for CYP activity under baseline conditions; in transparent 24-well plates (Greiner Bio-One; 55,000 cells per well in 500 μL) for RNA isolation and CYP induction studies; or in Transwell inserts (Corning; 25,000 cells per insert in 250 μL in the apical compartment (750 μL in the basolateral compartment); 0.4 μm pore 12 mm polyester membrane) for immunocytochemistry. ..

    Membrane:

    Article Title: Comparison of gene expression and biotransformation activity of HepaRG cells under static and dynamic culture conditions
    Article Snippet: .. For static culture conditions, cells were seeded in black coated 96-well plates (Greiner Bio-One, Frickenhausen, Germany; 9000 cells per well in 100 μL) for CYP activity under baseline conditions; in transparent 24-well plates (Greiner Bio-One; 55,000 cells per well in 500 μL) for RNA isolation and CYP induction studies; or in Transwell inserts (Corning; 25,000 cells per insert in 250 μL in the apical compartment (750 μL in the basolateral compartment); 0.4 μm pore 12 mm polyester membrane) for immunocytochemistry. ..

    Article Title: Malarial anemia: digestive vacuole of Plasmodium falciparum mediates complement deposition on bystander cells to provoke hemophagocytosis.
    Article Snippet: .. 1 3 Filter experiments Two-compartment culture plates (6.5-mm Transwell® with 3.0-μm pore polycarbonate membrane insert, Corning Incorporated, Corning, USA) were employed wherein the filters separated RBCs in the lower compartment from the DVs in the upper compartment, with active plasma present in both. ..

    Immunocytochemistry:

    Article Title: Comparison of gene expression and biotransformation activity of HepaRG cells under static and dynamic culture conditions
    Article Snippet: .. For static culture conditions, cells were seeded in black coated 96-well plates (Greiner Bio-One, Frickenhausen, Germany; 9000 cells per well in 100 μL) for CYP activity under baseline conditions; in transparent 24-well plates (Greiner Bio-One; 55,000 cells per well in 500 μL) for RNA isolation and CYP induction studies; or in Transwell inserts (Corning; 25,000 cells per insert in 250 μL in the apical compartment (750 μL in the basolateral compartment); 0.4 μm pore 12 mm polyester membrane) for immunocytochemistry. ..

    other:

    Article Title: Chronic hyperglycemia reduces the expression of intercellular adhesion molecules and increases intercellular hyperpermeability in the periodontal epithelium.
    Article Snippet: © 2023 John Wiley & Sons A/S.. Published by John Wiley & Sons Ltd. Yuki Narukawa, Naoyuki Sugiyama and Yoichiro Kashiwagi authors contributed equally to this work.. 1Department of Periodontology, Division of Oral Biology and Disease Control, Osaka University Graduate School of Dentistry, Osaka, Japan 2Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan 3Division of Interdisciplinary Dentistry, Osaka University Dental Hospital, Osaka, Japan 4Division of Metabolomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan

    Clinical Proteomics:

    Article Title: Malarial anemia: digestive vacuole of Plasmodium falciparum mediates complement deposition on bystander cells to provoke hemophagocytosis.
    Article Snippet: .. 1 3 Filter experiments Two-compartment culture plates (6.5-mm Transwell® with 3.0-μm pore polycarbonate membrane insert, Corning Incorporated, Corning, USA) were employed wherein the filters separated RBCs in the lower compartment from the DVs in the upper compartment, with active plasma present in both. ..



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    A) Experimental timeline of the conditioned place preference (CPP) paradigm. B) Illustration of the CPP apparatus in the low and high context version of the apparatus. In the low context version, the walls were distinctly patterned with horizontal stripes in the “left” compartment and zig zag stripes in the “right” compartment, but the flooring was smooth in both <t>compartments.</t> In the high context version, the flooring was also distinct between compartments, with the “left” compartment altered to a textured rubber flooring to distinguish it tactilely from the “right” compartment smooth flooring. C-D) % Time spent in the left compartment of the apparatus in the low ( C ) and high ( D ) context versions of the apparatus on the pretest, when mice could freely explore both compartments of the apparatus for the first time. Individual data points are color coded to reflect categorization of compartment bias on the pretest (pink: > 55%; teal: < 45%; black: between 45% and 55% in left compartment). *p < 0.05 for unpaired t-tests between males and females; # p < 0.05, #### p < 0.0001 for one-sample t-tests within group compared to the null hypothesis mean of 50%. E-F) Pretest locomotion in females and males, subcategorized by compartment bias of 55% as defined in C and D . Females had greater pretest locomotion than males in both the low ( E ) and high ( F ) context versions of the assay, but locomotion was unaffected by compartment bias. *p < 0.05, ****p < 0.0001 for main effects of sex in 2×2 ANOVAs.
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    A) Experimental timeline of the conditioned place preference (CPP) paradigm. B) Illustration of the CPP apparatus in the low and high context version of the apparatus. In the low context version, the walls were distinctly patterned with horizontal stripes in the “left” compartment and zig zag stripes in the “right” compartment, but the flooring was smooth in both <t>compartments.</t> In the high context version, the flooring was also distinct between compartments, with the “left” compartment altered to a textured rubber flooring to distinguish it tactilely from the “right” compartment smooth flooring. C-D) % Time spent in the left compartment of the apparatus in the low ( C ) and high ( D ) context versions of the apparatus on the pretest, when mice could freely explore both compartments of the apparatus for the first time. Individual data points are color coded to reflect categorization of compartment bias on the pretest (pink: > 55%; teal: < 45%; black: between 45% and 55% in left compartment). *p < 0.05 for unpaired t-tests between males and females; # p < 0.05, #### p < 0.0001 for one-sample t-tests within group compared to the null hypothesis mean of 50%. E-F) Pretest locomotion in females and males, subcategorized by compartment bias of 55% as defined in C and D . Females had greater pretest locomotion than males in both the low ( E ) and high ( F ) context versions of the assay, but locomotion was unaffected by compartment bias. *p < 0.05, ****p < 0.0001 for main effects of sex in 2×2 ANOVAs.
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    A) Experimental timeline of the conditioned place preference (CPP) paradigm. B) Illustration of the CPP apparatus in the low and high context version of the apparatus. In the low context version, the walls were distinctly patterned with horizontal stripes in the “left” compartment and zig zag stripes in the “right” compartment, but the flooring was smooth in both <t>compartments.</t> In the high context version, the flooring was also distinct between compartments, with the “left” compartment altered to a textured rubber flooring to distinguish it tactilely from the “right” compartment smooth flooring. C-D) % Time spent in the left compartment of the apparatus in the low ( C ) and high ( D ) context versions of the apparatus on the pretest, when mice could freely explore both compartments of the apparatus for the first time. Individual data points are color coded to reflect categorization of compartment bias on the pretest (pink: > 55%; teal: < 45%; black: between 45% and 55% in left compartment). *p < 0.05 for unpaired t-tests between males and females; # p < 0.05, #### p < 0.0001 for one-sample t-tests within group compared to the null hypothesis mean of 50%. E-F) Pretest locomotion in females and males, subcategorized by compartment bias of 55% as defined in C and D . Females had greater pretest locomotion than males in both the low ( E ) and high ( F ) context versions of the assay, but locomotion was unaffected by compartment bias. *p < 0.05, ****p < 0.0001 for main effects of sex in 2×2 ANOVAs.
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    A) Experimental timeline of the conditioned place preference (CPP) paradigm. B) Illustration of the CPP apparatus in the low and high context version of the apparatus. In the low context version, the walls were distinctly patterned with horizontal stripes in the “left” compartment and zig zag stripes in the “right” compartment, but the flooring was smooth in both <t>compartments.</t> In the high context version, the flooring was also distinct between compartments, with the “left” compartment altered to a textured rubber flooring to distinguish it tactilely from the “right” compartment smooth flooring. C-D) % Time spent in the left compartment of the apparatus in the low ( C ) and high ( D ) context versions of the apparatus on the pretest, when mice could freely explore both compartments of the apparatus for the first time. Individual data points are color coded to reflect categorization of compartment bias on the pretest (pink: > 55%; teal: < 45%; black: between 45% and 55% in left compartment). *p < 0.05 for unpaired t-tests between males and females; # p < 0.05, #### p < 0.0001 for one-sample t-tests within group compared to the null hypothesis mean of 50%. E-F) Pretest locomotion in females and males, subcategorized by compartment bias of 55% as defined in C and D . Females had greater pretest locomotion than males in both the low ( E ) and high ( F ) context versions of the assay, but locomotion was unaffected by compartment bias. *p < 0.05, ****p < 0.0001 for main effects of sex in 2×2 ANOVAs.
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    A) Experimental timeline of the conditioned place preference (CPP) paradigm. B) Illustration of the CPP apparatus in the low and high context version of the apparatus. In the low context version, the walls were distinctly patterned with horizontal stripes in the “left” compartment and zig zag stripes in the “right” compartment, but the flooring was smooth in both compartments. In the high context version, the flooring was also distinct between compartments, with the “left” compartment altered to a textured rubber flooring to distinguish it tactilely from the “right” compartment smooth flooring. C-D) % Time spent in the left compartment of the apparatus in the low ( C ) and high ( D ) context versions of the apparatus on the pretest, when mice could freely explore both compartments of the apparatus for the first time. Individual data points are color coded to reflect categorization of compartment bias on the pretest (pink: > 55%; teal: < 45%; black: between 45% and 55% in left compartment). *p < 0.05 for unpaired t-tests between males and females; # p < 0.05, #### p < 0.0001 for one-sample t-tests within group compared to the null hypothesis mean of 50%. E-F) Pretest locomotion in females and males, subcategorized by compartment bias of 55% as defined in C and D . Females had greater pretest locomotion than males in both the low ( E ) and high ( F ) context versions of the assay, but locomotion was unaffected by compartment bias. *p < 0.05, ****p < 0.0001 for main effects of sex in 2×2 ANOVAs.

    Journal: bioRxiv

    Article Title: Morphine-context associative memory and locomotor sensitization in mice are modulated by sex and context in a dose-dependent manner

    doi: 10.1101/2023.11.03.565492

    Figure Lengend Snippet: A) Experimental timeline of the conditioned place preference (CPP) paradigm. B) Illustration of the CPP apparatus in the low and high context version of the apparatus. In the low context version, the walls were distinctly patterned with horizontal stripes in the “left” compartment and zig zag stripes in the “right” compartment, but the flooring was smooth in both compartments. In the high context version, the flooring was also distinct between compartments, with the “left” compartment altered to a textured rubber flooring to distinguish it tactilely from the “right” compartment smooth flooring. C-D) % Time spent in the left compartment of the apparatus in the low ( C ) and high ( D ) context versions of the apparatus on the pretest, when mice could freely explore both compartments of the apparatus for the first time. Individual data points are color coded to reflect categorization of compartment bias on the pretest (pink: > 55%; teal: < 45%; black: between 45% and 55% in left compartment). *p < 0.05 for unpaired t-tests between males and females; # p < 0.05, #### p < 0.0001 for one-sample t-tests within group compared to the null hypothesis mean of 50%. E-F) Pretest locomotion in females and males, subcategorized by compartment bias of 55% as defined in C and D . Females had greater pretest locomotion than males in both the low ( E ) and high ( F ) context versions of the assay, but locomotion was unaffected by compartment bias. *p < 0.05, ****p < 0.0001 for main effects of sex in 2×2 ANOVAs.

    Article Snippet: The CPP apparatus consisted of a standard mouse arena (27.3×27.3×20.3 cm) separated into two compartments by a two chamber place preference insert with removable guillotine door (Med Associates Inc., Fairfax, VT, USA).

    Techniques: Conditioned Place Preference

    A-B) On the first day of conditioning (C1) in the low context ( A ) and high context ( B ) versions of the CPP assay, females displayed acute hyperlocomotion following the morphine injection on the afternoon conditioning session, regardless of whether the morphine was paired with the left or right compartment; this locomotor sensitivity was dose-dependent, as cohorts receiving higher doses of morphine displayed greater morphine-induced hyperlocomotion. Locomotion following saline injection on the morning session (6 hr earlier) was similar across morphine dose groups and paired compartment. C-D) Males displayed a similar dose-dependent hyperlocomotor response to morphine that was similar in both compartments of the apparatus in the low ( C ) and high ( D ) context assays, with no differences in saline locomotion. **p < 0.01, ****p < 0.0001 indicate main effect of morphine dose in 2×2 RM-ANOVAs; $$$ p ≤ 0.001, $$$$ p < 0.0001 indicate difference from 5 mg/kg morphine dose, ## p ≤ 0.01, ### p ≤ 0.001 indicates difference from 10 mg/kg morphine dose in post hoc t-tests between doses.

    Journal: bioRxiv

    Article Title: Morphine-context associative memory and locomotor sensitization in mice are modulated by sex and context in a dose-dependent manner

    doi: 10.1101/2023.11.03.565492

    Figure Lengend Snippet: A-B) On the first day of conditioning (C1) in the low context ( A ) and high context ( B ) versions of the CPP assay, females displayed acute hyperlocomotion following the morphine injection on the afternoon conditioning session, regardless of whether the morphine was paired with the left or right compartment; this locomotor sensitivity was dose-dependent, as cohorts receiving higher doses of morphine displayed greater morphine-induced hyperlocomotion. Locomotion following saline injection on the morning session (6 hr earlier) was similar across morphine dose groups and paired compartment. C-D) Males displayed a similar dose-dependent hyperlocomotor response to morphine that was similar in both compartments of the apparatus in the low ( C ) and high ( D ) context assays, with no differences in saline locomotion. **p < 0.01, ****p < 0.0001 indicate main effect of morphine dose in 2×2 RM-ANOVAs; $$$ p ≤ 0.001, $$$$ p < 0.0001 indicate difference from 5 mg/kg morphine dose, ## p ≤ 0.01, ### p ≤ 0.001 indicates difference from 10 mg/kg morphine dose in post hoc t-tests between doses.

    Article Snippet: The CPP apparatus consisted of a standard mouse arena (27.3×27.3×20.3 cm) separated into two compartments by a two chamber place preference insert with removable guillotine door (Med Associates Inc., Fairfax, VT, USA).

    Techniques: Injection, Saline