mouse e cad Search Results


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Enzyme Immunoassay for the Quantitative Determination of Mouse E-Cadherin, E-Cad in serum, plasma, tissues and other biological samples ?
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Cell lysate was prepared by homogenization of the over-expressed cells in ice-cold modified RIPA Lysis Buffer with cocktail of protease inhibitors (Sigma). Cell debris was removed by centrifugation. Protein concentration was determined by Bradford assay
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92
Elabscience Biotechnology e cadherin
E Cadherin, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+e+cad/Mouse+E-Cad+(E-Cadherin)+ELISA+Kit/pmc11340632-67-7-9
Average 92 stars, based on 1 article reviews
e cadherin - by Bioz Stars, 2026-09
92/100 stars
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94
Sino Biological recombinant his tag sinobiological 50671 m08h dapi sigma 10236276001 critical
Recombinant His Tag Sinobiological 50671 M08h Dapi Sigma 10236276001 Critical, supplied by Sino Biological, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+e+cad/Mouse+E-Cadherin+%2F+CDH1+%2F+E-cad+%2F+CD324+Protein/pm33725480-360-64-67
Average 94 stars, based on 1 article reviews
recombinant his tag sinobiological 50671 m08h dapi sigma 10236276001 critical - by Bioz Stars, 2026-09
94/100 stars
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90
Becton Dickinson monoclonal anti-mouse e-cadherin (e-cad
Collagen-supported epithelial sheets retain features of a fully differentiated epithelium. Murine (C57Bl/6) collagen-supported epithelial sheets and Matrigel ® embedded enteroids were cultured for 7–8 days, fixed, and stained for confocal microscopy. For (A) and (B) Z stack images were acquired and appropriate orthoslices of a single plane are shown to demonstrate staining localization. (A) Confocal images showing apical enrichment of F-actin (red) and basolateral localization of <t>E-cadherin</t> (green; scale bars = 20 μm). (B) Confocal images showing lateral expression of EpCAM (green; scale bar = 30 μm). (C) Confocal images showing localization of Paneth cells (LYZ; green) and goblet cells (MUC2; green) in collagen supported-epithelial sheets and Matrigel ® -grown enteroids (scale bars = 30 μm). (D) Graphs depict the proportion of enteroid epithelial cells expressing LYZ (Paneth cells; P < 0.05 by Student's unpaired t -test) or MUC2 (Goblet cells; P < 0.05 by Student's unpaired t -test) in 3D enteroids and collagen-supported epithelial sheets, respectively. Each data point indicates the mean of an individual experiment. Pooled data from at least three independent experiments per condition are shown. Mean ± SEM is shown. * indicates p <0.05.
Monoclonal Anti Mouse E Cadherin (E Cad, supplied by Becton Dickinson, 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/mouse+e+cad/monoclonal+anti+mouse+e+cadherin++e+cad/pmc06723115-126-25-30
Average 90 stars, based on 1 article reviews
monoclonal anti-mouse e-cadherin (e-cad - by Bioz Stars, 2026-09
90/100 stars
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This CLIA kit uses the Sandwich-CLIA principle. The micro CLIA plate provided in this kit has been pre-coated with an antibody specific to Mouse E-Cad. Samples or Standards are added to the micro CLIA plate
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Cadherins are calcium-dependent cell adhesion proteins which preferentially interact with themselves in a homophilic manner in connecting cells, and thus may contribute to the sorting of heterogeneous cell type. E-cadherin (E-Cad), also known as CDH1
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Mouse E-Cadherin,E-Cad ELISA Kit
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Image Search Results


Collagen-supported epithelial sheets retain features of a fully differentiated epithelium. Murine (C57Bl/6) collagen-supported epithelial sheets and Matrigel ® embedded enteroids were cultured for 7–8 days, fixed, and stained for confocal microscopy. For (A) and (B) Z stack images were acquired and appropriate orthoslices of a single plane are shown to demonstrate staining localization. (A) Confocal images showing apical enrichment of F-actin (red) and basolateral localization of E-cadherin (green; scale bars = 20 μm). (B) Confocal images showing lateral expression of EpCAM (green; scale bar = 30 μm). (C) Confocal images showing localization of Paneth cells (LYZ; green) and goblet cells (MUC2; green) in collagen supported-epithelial sheets and Matrigel ® -grown enteroids (scale bars = 30 μm). (D) Graphs depict the proportion of enteroid epithelial cells expressing LYZ (Paneth cells; P < 0.05 by Student's unpaired t -test) or MUC2 (Goblet cells; P < 0.05 by Student's unpaired t -test) in 3D enteroids and collagen-supported epithelial sheets, respectively. Each data point indicates the mean of an individual experiment. Pooled data from at least three independent experiments per condition are shown. Mean ± SEM is shown. * indicates p <0.05.

Journal: Frontiers in Cellular and Infection Microbiology

Article Title: An Open-Format Enteroid Culture System for Interrogation of Interactions Between Toxoplasma gondii and the Intestinal Epithelium

doi: 10.3389/fcimb.2019.00300

Figure Lengend Snippet: Collagen-supported epithelial sheets retain features of a fully differentiated epithelium. Murine (C57Bl/6) collagen-supported epithelial sheets and Matrigel ® embedded enteroids were cultured for 7–8 days, fixed, and stained for confocal microscopy. For (A) and (B) Z stack images were acquired and appropriate orthoslices of a single plane are shown to demonstrate staining localization. (A) Confocal images showing apical enrichment of F-actin (red) and basolateral localization of E-cadherin (green; scale bars = 20 μm). (B) Confocal images showing lateral expression of EpCAM (green; scale bar = 30 μm). (C) Confocal images showing localization of Paneth cells (LYZ; green) and goblet cells (MUC2; green) in collagen supported-epithelial sheets and Matrigel ® -grown enteroids (scale bars = 30 μm). (D) Graphs depict the proportion of enteroid epithelial cells expressing LYZ (Paneth cells; P < 0.05 by Student's unpaired t -test) or MUC2 (Goblet cells; P < 0.05 by Student's unpaired t -test) in 3D enteroids and collagen-supported epithelial sheets, respectively. Each data point indicates the mean of an individual experiment. Pooled data from at least three independent experiments per condition are shown. Mean ± SEM is shown. * indicates p <0.05.

Article Snippet: Primary antibodies used in this study include; monoclonal anti-mouse epithelial cell adhesion molecule (EpCAM; G8.8; Affymetrix eBiosciences), monoclonal anti-mouse lysozyme (LYZ; BGN/06/961; AbCam, Cambridge, UK), monoclonal anti-mouse e-cadherin (E-Cad; 24E10; BD Transduction Laboratories), polyclonal anti-mouse mucin-2 (MUC2; H-300; Insight Biotechnology), mouse anti- Toxoplasma gondii SAG1 membrane protein (TP3; AbCam), and anti- Toxoplasma gondii GRA7 (a kind gift from David Sibley, Washington University, St. Louis).

Techniques: Cell Culture, Staining, Confocal Microscopy, Expressing