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er marker calnexin  (Addgene inc)


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    Addgene inc er marker calnexin
    A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER <t>marker</t> <t>Calnexin.</t> G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.
    Er Marker Calnexin, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/er+marker+calnexin/mCherry-Calnexin-N-14+(Plasmid+%2355005)/bio_rxiv__2024__04__29__591613-135-18-30
    Average 93 stars, based on 8 article reviews
    er marker calnexin - by Bioz Stars, 2026-09
    93/100 stars

    Images

    1) Product Images from "Oligomerization and cellular localization of SLC26A11"

    Article Title: Oligomerization and cellular localization of SLC26A11

    Journal: bioRxiv

    doi: 10.1101/2024.04.29.591613

    A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER marker Calnexin. G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.
    Figure Legend Snippet: A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER marker Calnexin. G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.

    Techniques Used: Expressing, Marker, Transfection



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    A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER <t>marker</t> <t>Calnexin.</t> G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.
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    A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER <t>marker</t> <t>Calnexin.</t> G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.
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    A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER <t>marker</t> <t>Calnexin.</t> G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.
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    A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER <t>marker</t> <t>Calnexin.</t> G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.
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    Image Search Results


    A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER marker Calnexin. G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.

    Journal: bioRxiv

    Article Title: Oligomerization and cellular localization of SLC26A11

    doi: 10.1101/2024.04.29.591613

    Figure Lengend Snippet: A – F , Confocal images of HEK293T cells ( A, C and E ) and B-ICC Clone C cells ( B, D and F ) co-expressing SLC26A4/pendrin, SLC26A7 and SLC26A11 together with the lysosomal marker Lamp1 or the ER marker Calnexin. G and H , box plot of Manders coefficients of colocalization analysis between SLC26A4/pendrin, SLC26A7 and SLC26A11 with the corresponding intracellular marker (SLC26A11/Lamp1 HEK293T , n = 20; SLC26A11/Lamp1 CloneC , n = 20; SLC26A11/Calnexin HEK293T , n = 19; SLC26A11/Calnexin CloneC , n = 18); (SLC26A4/Lamp1 HEK293T , n = 20; SLC26A4/Lamp1 CloneC , n = 14; SLC26A4/Calnexin HEK293T , n = 18; SLC26A4/Calnexin CloneC , n = 15); (SLC26A7/Lamp1 HEK293T , n = 25; SLC26A7/Lamp1 CloneC , n = 23; SLC26A7/Calnexin HEK293T , n = 25; SLC26A7/Calnexin CloneC , n = 21); One-way ANOVA (Tukey’s HSD post hoc test). Data are presented as means ± S.D. with n being the number of co-transfected cells analyzed. In boxplots, boxes indicate the upper and lower quartiles, and whiskers the upper and lower 90 percentiles. Scale bars = 10 µm.

    Article Snippet: We received the lysosomal marker Lamp1 as a gift from Walter Mothes, Addgene plasmid #1817 , and the ER marker Calnexin as gift from Michael Davidson ( http://n2t.net/addgene:55005 ; RRID: Addgene_55005).

    Techniques: Expressing, Marker, Transfection