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claudin 1  (Thermo Fisher)


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    Structured Review

    Thermo Fisher claudin 1
    Distinct effects of bacterial siderophores (Ent, 2, 3-DHBA) and mammalian siderophore 2, 5-DHBA on mito-respiration and cell proliferation. (A) Schematic representation of the chemical structures of cyclic Ent (B) 2, 3-DHBA (C) 2, 5-DHBA (D) Seahorse XF analysis of mitochondrial respiration parameters in IEC treated with vehicle (control), Ent (25 μM), or 2, 3-DHBA (25 μM) or 2, 5-DHBA (25 μM). (E) Basal respiration, maximal respiratory capacity, and ATP production were quantified. (F) Quantification of mitochondrial ROS levels in treated cells, measured using MitoSOX TM fluorescence ( n = 5–6). (G) IEC were treated with Ent (25 µM) for 24 h to assess its impact on mRNA transcripts of tight junction proteins ( ZO-1, occludin , <t>and</t> <t>claudin-1</t> ) involved in epithelial barrier integrity via qRT-PCR. (H) Confluent monolayers of IEC were scratched and treated with 25 µM of indicated siderophores, and wound closure was monitored and imaged at each time point using phase-contrast microscopy through Incucyte (I) Quantification of wound area showed a time-dependent inhibition of wound healing in Ent-treated cells compared to untreated controls ( n = 6–7). Data represent SEM from n = 3 biological replicates, with each biological replicate plated in 5–6 technical wells. Statistical significance was determined by one-way ANOVA with post hoc analysis (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001).
    Claudin 1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/storage+tubes/Racks+for+Matrix+2D+Barcoded+Storage+Tubes/pmc13114135-44-17-21
    Average 95 stars, based on 1 article reviews
    claudin 1 - by Bioz Stars, 2026-09
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    Images

    1) Product Images from "Microbial metabolite Enterobactin impairs mitochondrial respiration and alleviates colitis"

    Article Title: Microbial metabolite Enterobactin impairs mitochondrial respiration and alleviates colitis

    Journal: Gut Microbes

    doi: 10.1080/19490976.2026.2662638

    Distinct effects of bacterial siderophores (Ent, 2, 3-DHBA) and mammalian siderophore 2, 5-DHBA on mito-respiration and cell proliferation. (A) Schematic representation of the chemical structures of cyclic Ent (B) 2, 3-DHBA (C) 2, 5-DHBA (D) Seahorse XF analysis of mitochondrial respiration parameters in IEC treated with vehicle (control), Ent (25 μM), or 2, 3-DHBA (25 μM) or 2, 5-DHBA (25 μM). (E) Basal respiration, maximal respiratory capacity, and ATP production were quantified. (F) Quantification of mitochondrial ROS levels in treated cells, measured using MitoSOX TM fluorescence ( n = 5–6). (G) IEC were treated with Ent (25 µM) for 24 h to assess its impact on mRNA transcripts of tight junction proteins ( ZO-1, occludin , and claudin-1 ) involved in epithelial barrier integrity via qRT-PCR. (H) Confluent monolayers of IEC were scratched and treated with 25 µM of indicated siderophores, and wound closure was monitored and imaged at each time point using phase-contrast microscopy through Incucyte (I) Quantification of wound area showed a time-dependent inhibition of wound healing in Ent-treated cells compared to untreated controls ( n = 6–7). Data represent SEM from n = 3 biological replicates, with each biological replicate plated in 5–6 technical wells. Statistical significance was determined by one-way ANOVA with post hoc analysis (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001).
    Figure Legend Snippet: Distinct effects of bacterial siderophores (Ent, 2, 3-DHBA) and mammalian siderophore 2, 5-DHBA on mito-respiration and cell proliferation. (A) Schematic representation of the chemical structures of cyclic Ent (B) 2, 3-DHBA (C) 2, 5-DHBA (D) Seahorse XF analysis of mitochondrial respiration parameters in IEC treated with vehicle (control), Ent (25 μM), or 2, 3-DHBA (25 μM) or 2, 5-DHBA (25 μM). (E) Basal respiration, maximal respiratory capacity, and ATP production were quantified. (F) Quantification of mitochondrial ROS levels in treated cells, measured using MitoSOX TM fluorescence ( n = 5–6). (G) IEC were treated with Ent (25 µM) for 24 h to assess its impact on mRNA transcripts of tight junction proteins ( ZO-1, occludin , and claudin-1 ) involved in epithelial barrier integrity via qRT-PCR. (H) Confluent monolayers of IEC were scratched and treated with 25 µM of indicated siderophores, and wound closure was monitored and imaged at each time point using phase-contrast microscopy through Incucyte (I) Quantification of wound area showed a time-dependent inhibition of wound healing in Ent-treated cells compared to untreated controls ( n = 6–7). Data represent SEM from n = 3 biological replicates, with each biological replicate plated in 5–6 technical wells. Statistical significance was determined by one-way ANOVA with post hoc analysis (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001).

    Techniques Used: Control, Fluorescence, Quantitative RT-PCR, Microscopy, Inhibition

    Monomeric Ent, 2, 3-DHBA, but not 2, 5-DHBA, restores mucosal integrity and mitochondrial homeostasis in DSS-induced colitis. Acute colitis was induced in mice as in Figure 7. After the cessation of DSS (recovery phase) mice were given either 2, 3-DHBA or 2, 5-DHBA (500 µg/mouse per day) for 7 d and euthanized. (A) Representative H&E-stained colon sections showing epithelial damage, crypt loss, and inflammatory cells ( n = 5/group). (B) Alcian blue staining for goblet cells in the colon (C) Immunoblot analysis of tight junction proteins (occludin and claudin-1) in colonic tissue. (D) qRT-PCR analysis of genes involved in mitochondrial biogenesis peroxisome proliferator activated receptor gamma coactivator 1-alpha ( PGC-1α ) and deiodinase type 2 ( Dio2) .(E) Colonic expression of antioxidant genes (Superoxide dismutase 2 (SOD2) , glutathione peroxidase (Gpx) , and nuclear factor erythroid 2-related factor 2 (Nrf2) (F) Immunoblot showing protein involved in mitochondrial dynamics uncoupling protein 1 (Ucp1), mitofusin 1 (Mfn1), and optic atrophy type 1 (Opa1). Data is presented as mean ± SEM ( n = 5). Statistical comparisons were performed using one-way ANOVA with Tukey’s post hoc test (* p < 0.05, ** p < 0.01, and *** p < 0.001).
    Figure Legend Snippet: Monomeric Ent, 2, 3-DHBA, but not 2, 5-DHBA, restores mucosal integrity and mitochondrial homeostasis in DSS-induced colitis. Acute colitis was induced in mice as in Figure 7. After the cessation of DSS (recovery phase) mice were given either 2, 3-DHBA or 2, 5-DHBA (500 µg/mouse per day) for 7 d and euthanized. (A) Representative H&E-stained colon sections showing epithelial damage, crypt loss, and inflammatory cells ( n = 5/group). (B) Alcian blue staining for goblet cells in the colon (C) Immunoblot analysis of tight junction proteins (occludin and claudin-1) in colonic tissue. (D) qRT-PCR analysis of genes involved in mitochondrial biogenesis peroxisome proliferator activated receptor gamma coactivator 1-alpha ( PGC-1α ) and deiodinase type 2 ( Dio2) .(E) Colonic expression of antioxidant genes (Superoxide dismutase 2 (SOD2) , glutathione peroxidase (Gpx) , and nuclear factor erythroid 2-related factor 2 (Nrf2) (F) Immunoblot showing protein involved in mitochondrial dynamics uncoupling protein 1 (Ucp1), mitofusin 1 (Mfn1), and optic atrophy type 1 (Opa1). Data is presented as mean ± SEM ( n = 5). Statistical comparisons were performed using one-way ANOVA with Tukey’s post hoc test (* p < 0.05, ** p < 0.01, and *** p < 0.001).

    Techniques Used: Staining, Western Blot, Quantitative RT-PCR, Expressing

    Related Articles

    Cell Culture:

    Article Title: Maternal human papillomavirus infections at mid-pregnancy and delivery in a Scandinavian mother-child cohort study.
    Article Snippet: HPV sampling and analyses First-void urine samples collected, in 70 ml urine sample containers (Sarstedt™, Nümbrecht, Germany), at mid-gestation and delivery were used for HPV analyses. .. Samples were stored at 4°C immediately after collection and, within 30 hours, 4.5 ml were transferred to storage tubes (Biobanking and Cell Culture Cryogenic tubes (Nunc, Thermo ScientificTM, Waltham, MA, USA) and kept frozen at -80°C up to 36 months until analysis. .. Total nucleic acids were extracted from 1000 μl thawed vortexed urine using the generic protocol on NucliSENS© easyMAG© (BioMerieux SA, Marcy l’Etoile, France), eluted in 50 μl elution buffer, and kept frozen at -80°C until analysis.

    Isolation:

    Article Title: Submicron Size Particles of a Murine Monoclonal Antibody Are More Immunogenic Than Soluble Oligomers or Micron Size Particles Upon Subcutaneous Administration in Mice.
    Article Snippet: Blood was collected into the MiniCollect® Serum Z separator tubes (Greiner Bio-One, Alphen aan den Rijn, The Netherlands). .. Serum was isolated by centrifugation (3000 g, 10 min), collected into storage tubes (Thermo Fisher Scientific) and kept at 80 C for analysis. .. The ADA screening was performed with a bridging ELISA according to an adopted protocol previously described by Qiu et al.29 The capture and detection reagents, mIgG1-biotin and mIgG1digoxigenin, were obtained by labeling of mIgG1 with EZ-Link® sulfo-NHS-LC-biotin (Thermo Fisher Scientific) or 3-amino-3deoxydigoxigenin hemisuccinamide, succinimidyl ester (Thermo Fisher Scientific) according to the manufacturer's protocols.

    Article Title: Monoclonal Antibody Dimers Induced by Low pH, Heat, or Light Exposure Are Not Immunogenic Upon Subcutaneous Administration in a Mouse Model.
    Article Snippet: Blood was collected into the MiniCollect® Serum Z separator tubes (Greiner Bio-One). .. Serum was isolated by centrifugation (3000 g, 10 min, 4 C), collected into storage tubes (Thermo Fisher Scientific), and kept at 80 C for analysis. ..

    Centrifugation:

    Article Title: Submicron Size Particles of a Murine Monoclonal Antibody Are More Immunogenic Than Soluble Oligomers or Micron Size Particles Upon Subcutaneous Administration in Mice.
    Article Snippet: Blood was collected into the MiniCollect® Serum Z separator tubes (Greiner Bio-One, Alphen aan den Rijn, The Netherlands). .. Serum was isolated by centrifugation (3000 g, 10 min), collected into storage tubes (Thermo Fisher Scientific) and kept at 80 C for analysis. .. The ADA screening was performed with a bridging ELISA according to an adopted protocol previously described by Qiu et al.29 The capture and detection reagents, mIgG1-biotin and mIgG1digoxigenin, were obtained by labeling of mIgG1 with EZ-Link® sulfo-NHS-LC-biotin (Thermo Fisher Scientific) or 3-amino-3deoxydigoxigenin hemisuccinamide, succinimidyl ester (Thermo Fisher Scientific) according to the manufacturer's protocols.

    Article Title: Monoclonal Antibody Dimers Induced by Low pH, Heat, or Light Exposure Are Not Immunogenic Upon Subcutaneous Administration in a Mouse Model.
    Article Snippet: Blood was collected into the MiniCollect® Serum Z separator tubes (Greiner Bio-One). .. Serum was isolated by centrifugation (3000 g, 10 min, 4 C), collected into storage tubes (Thermo Fisher Scientific), and kept at 80 C for analysis. ..

    Transferring:

    Article Title: AmSty, Ineos, Trinseo to recycle polystyrene
    Article Snippet: Ansa Biotechnologies has raised $7.9 million in seed financing, bringing its funding to date to $9.2 million.. The California-based company synthesizes DNA with a fully enzymatic process that it claims results in longer, higher-quality strands than DNA made with phosphoramidite chemistry, which limits assembled DNA to about 200 base pairs.. Firms like Ansa and Molecular Assemblies, founded in 2013, say enzymes can make the longer DNA BIOBASED CHEMICALS

    Bioprocessing:

    Article Title: AmSty, Ineos, Trinseo to recycle polystyrene
    Article Snippet: Ansa Biotechnologies has raised $7.9 million in seed financing, bringing its funding to date to $9.2 million.. The California-based company synthesizes DNA with a fully enzymatic process that it claims results in longer, higher-quality strands than DNA made with phosphoramidite chemistry, which limits assembled DNA to about 200 base pairs.. Firms like Ansa and Molecular Assemblies, founded in 2013, say enzymes can make the longer DNA BIOBASED CHEMICALS



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    Distinct effects of bacterial siderophores (Ent, 2, 3-DHBA) and mammalian siderophore 2, 5-DHBA on mito-respiration and cell proliferation. (A) Schematic representation of the chemical structures of cyclic Ent (B) 2, 3-DHBA (C) 2, 5-DHBA (D) Seahorse XF analysis of mitochondrial respiration parameters in IEC treated with vehicle (control), Ent (25 μM), or 2, 3-DHBA (25 μM) or 2, 5-DHBA (25 μM). (E) Basal respiration, maximal respiratory capacity, and ATP production were quantified. (F) Quantification of mitochondrial ROS levels in treated cells, measured using MitoSOX TM fluorescence ( n = 5–6). (G) IEC were treated with Ent (25 µM) for 24 h to assess its impact on mRNA transcripts of tight junction proteins ( ZO-1, occludin , <t>and</t> <t>claudin-1</t> ) involved in epithelial barrier integrity via qRT-PCR. (H) Confluent monolayers of IEC were scratched and treated with 25 µM of indicated siderophores, and wound closure was monitored and imaged at each time point using phase-contrast microscopy through Incucyte (I) Quantification of wound area showed a time-dependent inhibition of wound healing in Ent-treated cells compared to untreated controls ( n = 6–7). Data represent SEM from n = 3 biological replicates, with each biological replicate plated in 5–6 technical wells. Statistical significance was determined by one-way ANOVA with post hoc analysis (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001).
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    Distinct effects of bacterial siderophores (Ent, 2, 3-DHBA) and mammalian siderophore 2, 5-DHBA on mito-respiration and cell proliferation. (A) Schematic representation of the chemical structures of cyclic Ent (B) 2, 3-DHBA (C) 2, 5-DHBA (D) Seahorse XF analysis of mitochondrial respiration parameters in IEC treated with vehicle (control), Ent (25 μM), or 2, 3-DHBA (25 μM) or 2, 5-DHBA (25 μM). (E) Basal respiration, maximal respiratory capacity, and ATP production were quantified. (F) Quantification of mitochondrial ROS levels in treated cells, measured using MitoSOX TM fluorescence ( n = 5–6). (G) IEC were treated with Ent (25 µM) for 24 h to assess its impact on mRNA transcripts of tight junction proteins ( ZO-1, occludin , <t>and</t> <t>claudin-1</t> ) involved in epithelial barrier integrity via qRT-PCR. (H) Confluent monolayers of IEC were scratched and treated with 25 µM of indicated siderophores, and wound closure was monitored and imaged at each time point using phase-contrast microscopy through Incucyte (I) Quantification of wound area showed a time-dependent inhibition of wound healing in Ent-treated cells compared to untreated controls ( n = 6–7). Data represent SEM from n = 3 biological replicates, with each biological replicate plated in 5–6 technical wells. Statistical significance was determined by one-way ANOVA with post hoc analysis (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001).
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    Distinct effects of bacterial siderophores (Ent, 2, 3-DHBA) and mammalian siderophore 2, 5-DHBA on mito-respiration and cell proliferation. (A) Schematic representation of the chemical structures of cyclic Ent (B) 2, 3-DHBA (C) 2, 5-DHBA (D) Seahorse XF analysis of mitochondrial respiration parameters in IEC treated with vehicle (control), Ent (25 μM), or 2, 3-DHBA (25 μM) or 2, 5-DHBA (25 μM). (E) Basal respiration, maximal respiratory capacity, and ATP production were quantified. (F) Quantification of mitochondrial ROS levels in treated cells, measured using MitoSOX TM fluorescence ( n = 5–6). (G) IEC were treated with Ent (25 µM) for 24 h to assess its impact on mRNA transcripts of tight junction proteins ( ZO-1, occludin , <t>and</t> <t>claudin-1</t> ) involved in epithelial barrier integrity via qRT-PCR. (H) Confluent monolayers of IEC were scratched and treated with 25 µM of indicated siderophores, and wound closure was monitored and imaged at each time point using phase-contrast microscopy through Incucyte (I) Quantification of wound area showed a time-dependent inhibition of wound healing in Ent-treated cells compared to untreated controls ( n = 6–7). Data represent SEM from n = 3 biological replicates, with each biological replicate plated in 5–6 technical wells. Statistical significance was determined by one-way ANOVA with post hoc analysis (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001).
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    Distinct effects of bacterial siderophores (Ent, 2, 3-DHBA) and mammalian siderophore 2, 5-DHBA on mito-respiration and cell proliferation. (A) Schematic representation of the chemical structures of cyclic Ent (B) 2, 3-DHBA (C) 2, 5-DHBA (D) Seahorse XF analysis of mitochondrial respiration parameters in IEC treated with vehicle (control), Ent (25 μM), or 2, 3-DHBA (25 μM) or 2, 5-DHBA (25 μM). (E) Basal respiration, maximal respiratory capacity, and ATP production were quantified. (F) Quantification of mitochondrial ROS levels in treated cells, measured using MitoSOX TM fluorescence ( n = 5–6). (G) IEC were treated with Ent (25 µM) for 24 h to assess its impact on mRNA transcripts of tight junction proteins ( ZO-1, occludin , and claudin-1 ) involved in epithelial barrier integrity via qRT-PCR. (H) Confluent monolayers of IEC were scratched and treated with 25 µM of indicated siderophores, and wound closure was monitored and imaged at each time point using phase-contrast microscopy through Incucyte (I) Quantification of wound area showed a time-dependent inhibition of wound healing in Ent-treated cells compared to untreated controls ( n = 6–7). Data represent SEM from n = 3 biological replicates, with each biological replicate plated in 5–6 technical wells. Statistical significance was determined by one-way ANOVA with post hoc analysis (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001).

    Journal: Gut Microbes

    Article Title: Microbial metabolite Enterobactin impairs mitochondrial respiration and alleviates colitis

    doi: 10.1080/19490976.2026.2662638

    Figure Lengend Snippet: Distinct effects of bacterial siderophores (Ent, 2, 3-DHBA) and mammalian siderophore 2, 5-DHBA on mito-respiration and cell proliferation. (A) Schematic representation of the chemical structures of cyclic Ent (B) 2, 3-DHBA (C) 2, 5-DHBA (D) Seahorse XF analysis of mitochondrial respiration parameters in IEC treated with vehicle (control), Ent (25 μM), or 2, 3-DHBA (25 μM) or 2, 5-DHBA (25 μM). (E) Basal respiration, maximal respiratory capacity, and ATP production were quantified. (F) Quantification of mitochondrial ROS levels in treated cells, measured using MitoSOX TM fluorescence ( n = 5–6). (G) IEC were treated with Ent (25 µM) for 24 h to assess its impact on mRNA transcripts of tight junction proteins ( ZO-1, occludin , and claudin-1 ) involved in epithelial barrier integrity via qRT-PCR. (H) Confluent monolayers of IEC were scratched and treated with 25 µM of indicated siderophores, and wound closure was monitored and imaged at each time point using phase-contrast microscopy through Incucyte (I) Quantification of wound area showed a time-dependent inhibition of wound healing in Ent-treated cells compared to untreated controls ( n = 6–7). Data represent SEM from n = 3 biological replicates, with each biological replicate plated in 5–6 technical wells. Statistical significance was determined by one-way ANOVA with post hoc analysis (* p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001).

    Article Snippet: Antibodies to OXPHOS (Catalog # 45-8099) were from Thermo Fischer, and antibodies to occludin (Catalog #40-4700) and claudin-1 (Catalog #37-4900) from Invitrogen and UCP1 (Catalog #MAB6158) from R&D Systems.

    Techniques: Control, Fluorescence, Quantitative RT-PCR, Microscopy, Inhibition

    Monomeric Ent, 2, 3-DHBA, but not 2, 5-DHBA, restores mucosal integrity and mitochondrial homeostasis in DSS-induced colitis. Acute colitis was induced in mice as in Figure 7. After the cessation of DSS (recovery phase) mice were given either 2, 3-DHBA or 2, 5-DHBA (500 µg/mouse per day) for 7 d and euthanized. (A) Representative H&E-stained colon sections showing epithelial damage, crypt loss, and inflammatory cells ( n = 5/group). (B) Alcian blue staining for goblet cells in the colon (C) Immunoblot analysis of tight junction proteins (occludin and claudin-1) in colonic tissue. (D) qRT-PCR analysis of genes involved in mitochondrial biogenesis peroxisome proliferator activated receptor gamma coactivator 1-alpha ( PGC-1α ) and deiodinase type 2 ( Dio2) .(E) Colonic expression of antioxidant genes (Superoxide dismutase 2 (SOD2) , glutathione peroxidase (Gpx) , and nuclear factor erythroid 2-related factor 2 (Nrf2) (F) Immunoblot showing protein involved in mitochondrial dynamics uncoupling protein 1 (Ucp1), mitofusin 1 (Mfn1), and optic atrophy type 1 (Opa1). Data is presented as mean ± SEM ( n = 5). Statistical comparisons were performed using one-way ANOVA with Tukey’s post hoc test (* p < 0.05, ** p < 0.01, and *** p < 0.001).

    Journal: Gut Microbes

    Article Title: Microbial metabolite Enterobactin impairs mitochondrial respiration and alleviates colitis

    doi: 10.1080/19490976.2026.2662638

    Figure Lengend Snippet: Monomeric Ent, 2, 3-DHBA, but not 2, 5-DHBA, restores mucosal integrity and mitochondrial homeostasis in DSS-induced colitis. Acute colitis was induced in mice as in Figure 7. After the cessation of DSS (recovery phase) mice were given either 2, 3-DHBA or 2, 5-DHBA (500 µg/mouse per day) for 7 d and euthanized. (A) Representative H&E-stained colon sections showing epithelial damage, crypt loss, and inflammatory cells ( n = 5/group). (B) Alcian blue staining for goblet cells in the colon (C) Immunoblot analysis of tight junction proteins (occludin and claudin-1) in colonic tissue. (D) qRT-PCR analysis of genes involved in mitochondrial biogenesis peroxisome proliferator activated receptor gamma coactivator 1-alpha ( PGC-1α ) and deiodinase type 2 ( Dio2) .(E) Colonic expression of antioxidant genes (Superoxide dismutase 2 (SOD2) , glutathione peroxidase (Gpx) , and nuclear factor erythroid 2-related factor 2 (Nrf2) (F) Immunoblot showing protein involved in mitochondrial dynamics uncoupling protein 1 (Ucp1), mitofusin 1 (Mfn1), and optic atrophy type 1 (Opa1). Data is presented as mean ± SEM ( n = 5). Statistical comparisons were performed using one-way ANOVA with Tukey’s post hoc test (* p < 0.05, ** p < 0.01, and *** p < 0.001).

    Article Snippet: Antibodies to OXPHOS (Catalog # 45-8099) were from Thermo Fischer, and antibodies to occludin (Catalog #40-4700) and claudin-1 (Catalog #37-4900) from Invitrogen and UCP1 (Catalog #MAB6158) from R&D Systems.

    Techniques: Staining, Western Blot, Quantitative RT-PCR, Expressing