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primary antibodies mucin2  (Servicebio Inc)

 
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    Servicebio Inc primary antibodies mucin2
    Primary Antibodies Mucin2, supplied by Servicebio Inc, 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/result/primary antibodies mucin2/product/Servicebio Inc
    Average 90 stars, based on 1 article reviews
    primary antibodies mucin2 - by Bioz Stars, 2026-05
    90/100 stars

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    primary antibodies mucin2  (Servicebio Inc)
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    rabbit anti-mucin2 primary antibody #sc-15,334  (Santa Cruz Biotechnology)
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    Evaluation of human, small intestinal monolayer systems. a Schematic and fluorescence side images of the gradient cross-linked scaffold (top) and conventional scaffold overlaying a porous membrane (bottom). Scale bar = 300 μm. b Fluorescence images of the monolayers at day 10 stained for EdU (green), ALP (red), <t>Muc2</t> (yellow), and nuclei (blue). Scale bar = 100 μm. c Quantification of Edu, ALP, and Muc2 on day 5 and day 10 of culture as a percentage of the Hoechst 33342 (nuclei stain) positive area ( n = 3). Edu, ALP, and Muc2 expression was not statistically different between the two monolayer systems in EM or DM
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    Evaluation of human, small intestinal monolayer systems. a Schematic and fluorescence side images of the gradient cross-linked scaffold (top) and conventional scaffold overlaying a porous membrane (bottom). Scale bar = 300 μm. b Fluorescence images of the monolayers at day 10 stained for EdU (green), ALP (red), <t>Muc2</t> (yellow), and nuclei (blue). Scale bar = 100 μm. c Quantification of Edu, ALP, and Muc2 on day 5 and day 10 of culture as a percentage of the Hoechst 33342 (nuclei stain) positive area ( n = 3). Edu, ALP, and Muc2 expression was not statistically different between the two monolayer systems in EM or DM
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    primary antibodies α mucin2  (Santa Cruz Biotechnology)
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    Evaluation of human, small intestinal monolayer systems. a Schematic and fluorescence side images of the gradient cross-linked scaffold (top) and conventional scaffold overlaying a porous membrane (bottom). Scale bar = 300 μm. b Fluorescence images of the monolayers at day 10 stained for EdU (green), ALP (red), <t>Muc2</t> (yellow), and nuclei (blue). Scale bar = 100 μm. c Quantification of Edu, ALP, and Muc2 on day 5 and day 10 of culture as a percentage of the Hoechst 33342 (nuclei stain) positive area ( n = 3). Edu, ALP, and Muc2 expression was not statistically different between the two monolayer systems in EM or DM
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    Evaluation of human, small intestinal monolayer systems. a Schematic and fluorescence side images of the gradient cross-linked scaffold (top) and conventional scaffold overlaying a porous membrane (bottom). Scale bar = 300 μm. b Fluorescence images of the monolayers at day 10 stained for EdU (green), ALP (red), Muc2 (yellow), and nuclei (blue). Scale bar = 100 μm. c Quantification of Edu, ALP, and Muc2 on day 5 and day 10 of culture as a percentage of the Hoechst 33342 (nuclei stain) positive area ( n = 3). Edu, ALP, and Muc2 expression was not statistically different between the two monolayer systems in EM or DM

    Journal: Journal of Biological Engineering

    Article Title: Molecular transport through primary human small intestinal monolayers by culture on a collagen scaffold with a gradient of chemical cross-linking

    doi: 10.1186/s13036-019-0165-4

    Figure Lengend Snippet: Evaluation of human, small intestinal monolayer systems. a Schematic and fluorescence side images of the gradient cross-linked scaffold (top) and conventional scaffold overlaying a porous membrane (bottom). Scale bar = 300 μm. b Fluorescence images of the monolayers at day 10 stained for EdU (green), ALP (red), Muc2 (yellow), and nuclei (blue). Scale bar = 100 μm. c Quantification of Edu, ALP, and Muc2 on day 5 and day 10 of culture as a percentage of the Hoechst 33342 (nuclei stain) positive area ( n = 3). Edu, ALP, and Muc2 expression was not statistically different between the two monolayer systems in EM or DM

    Article Snippet: The fixed cells were analyzed for the presence of mucin-2 (Muc2) by immunostaining with a rabbit anti-mucin2 primary antibody (α-muc2, 1:200, Santa Cruz Biotechnology, Dallas, TX, #sc-15,334) followed by an Alexa Fluor 488 α-rabbit secondary antibody (1:500, Jackson Immunoresearch, West Grove, PA, # 711–545-152).

    Techniques: Fluorescence, Membrane, Staining, Expressing