Review



glut2  (Bioss)


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    Structured Review

    Bioss glut2
    NaB ameliorated high glucose- and LPS-induced damage in CaCo 2 cells. ( A ) Insulin, ( B ) LPS, and ( C ) sodium butyrate (NaB) concentration-dependently inhibited CaCo 2 cell viability, * p < 0.05, ** p < 0.01, *** p < 0.001, vs. control, n = 3. Immunofluorescence assays for ( D ) GPR43, ( E ) <t>GLUT2,</t> and ( F ) insulin receptor (IR) under a laser scanning confocal microscope and ( G – J ) relative fluorescence intensity were determined. * p < 0.05, ** p < 0.01, *** p < 0.001, vs. Ins + LPS, n = 3.
    Glut2, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/glut2/product/Bioss
    Average 94 stars, based on 20 article reviews
    glut2 - by Bioz Stars, 2026-02
    94/100 stars

    Images

    1) Product Images from "Sodium Butyrate Ameliorated Bile Acid Metabolism in Diabetes Mellitus by PI3K/AKT Signaling Pathway via the Gut–Liver Axis"

    Article Title: Sodium Butyrate Ameliorated Bile Acid Metabolism in Diabetes Mellitus by PI3K/AKT Signaling Pathway via the Gut–Liver Axis

    Journal: Current Issues in Molecular Biology

    doi: 10.3390/cimb47090732

    NaB ameliorated high glucose- and LPS-induced damage in CaCo 2 cells. ( A ) Insulin, ( B ) LPS, and ( C ) sodium butyrate (NaB) concentration-dependently inhibited CaCo 2 cell viability, * p < 0.05, ** p < 0.01, *** p < 0.001, vs. control, n = 3. Immunofluorescence assays for ( D ) GPR43, ( E ) GLUT2, and ( F ) insulin receptor (IR) under a laser scanning confocal microscope and ( G – J ) relative fluorescence intensity were determined. * p < 0.05, ** p < 0.01, *** p < 0.001, vs. Ins + LPS, n = 3.
    Figure Legend Snippet: NaB ameliorated high glucose- and LPS-induced damage in CaCo 2 cells. ( A ) Insulin, ( B ) LPS, and ( C ) sodium butyrate (NaB) concentration-dependently inhibited CaCo 2 cell viability, * p < 0.05, ** p < 0.01, *** p < 0.001, vs. control, n = 3. Immunofluorescence assays for ( D ) GPR43, ( E ) GLUT2, and ( F ) insulin receptor (IR) under a laser scanning confocal microscope and ( G – J ) relative fluorescence intensity were determined. * p < 0.05, ** p < 0.01, *** p < 0.001, vs. Ins + LPS, n = 3.

    Techniques Used: Concentration Assay, Control, Immunofluorescence, Microscopy, Fluorescence



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    NaB ameliorated high glucose- and LPS-induced damage in CaCo 2 cells. ( A ) Insulin, ( B ) LPS, and ( C ) sodium butyrate (NaB) concentration-dependently inhibited CaCo 2 cell viability, * p < 0.05, ** p < 0.01, *** p < 0.001, vs. control, n = 3. Immunofluorescence assays for ( D ) GPR43, ( E ) <t>GLUT2,</t> and ( F ) insulin receptor (IR) under a laser scanning confocal microscope and ( G – J ) relative fluorescence intensity were determined. * p < 0.05, ** p < 0.01, *** p < 0.001, vs. Ins + LPS, n = 3.
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    Image Search Results


    NaB ameliorated high glucose- and LPS-induced damage in CaCo 2 cells. ( A ) Insulin, ( B ) LPS, and ( C ) sodium butyrate (NaB) concentration-dependently inhibited CaCo 2 cell viability, * p < 0.05, ** p < 0.01, *** p < 0.001, vs. control, n = 3. Immunofluorescence assays for ( D ) GPR43, ( E ) GLUT2, and ( F ) insulin receptor (IR) under a laser scanning confocal microscope and ( G – J ) relative fluorescence intensity were determined. * p < 0.05, ** p < 0.01, *** p < 0.001, vs. Ins + LPS, n = 3.

    Journal: Current Issues in Molecular Biology

    Article Title: Sodium Butyrate Ameliorated Bile Acid Metabolism in Diabetes Mellitus by PI3K/AKT Signaling Pathway via the Gut–Liver Axis

    doi: 10.3390/cimb47090732

    Figure Lengend Snippet: NaB ameliorated high glucose- and LPS-induced damage in CaCo 2 cells. ( A ) Insulin, ( B ) LPS, and ( C ) sodium butyrate (NaB) concentration-dependently inhibited CaCo 2 cell viability, * p < 0.05, ** p < 0.01, *** p < 0.001, vs. control, n = 3. Immunofluorescence assays for ( D ) GPR43, ( E ) GLUT2, and ( F ) insulin receptor (IR) under a laser scanning confocal microscope and ( G – J ) relative fluorescence intensity were determined. * p < 0.05, ** p < 0.01, *** p < 0.001, vs. Ins + LPS, n = 3.

    Article Snippet: Primary antibodies against GPR43 (bs-13536R), PTPN6 (bs-4158R), GATA4 (bs-1778R), GLUT2 (bs-0351R), Insulin Receptor (bs-0681R), PI3K (bs-10657R), and p-PI3K (bs-6417R) were obtained from Bioss (Peking, China).

    Techniques: Concentration Assay, Control, Immunofluorescence, Microscopy, Fluorescence