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primary antibodies against endogenous hnf1a protein  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology primary antibodies against endogenous hnf1a protein
    Primary Antibodies Against Endogenous Hnf1a Protein, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 189 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+antibodies+against+endogenous+hnf1a+protein/HNF-1%CE%B1+Antibody/pm34035238-374-0-6
    Average 93 stars, based on 189 article reviews
    primary antibodies against endogenous hnf1a protein - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Functional Assay:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Binding Assay:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Mutagenesis:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Sequencing:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Quantitative RT-PCR:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Flow Cytometry:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Expressing:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Derivative Assay:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Reverse Transcription:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Polymerase Chain Reaction:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    One-tailed Test:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    RNA Sequencing:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Gene Expression:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    MANN-WHITNEY:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    ChIP-sequencing:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Transfection:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Negative Control:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Western Blot:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Construct:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Immunohistochemistry:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Staining:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Immunofluorescence:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Cell Counting:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Luciferase:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Activity Assay:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    ChIP-qPCR:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Comparison:

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells.
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).

    Article Title: Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
    Article Snippet: Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).Protein lysates were quantified using the BCA Assay (Thermo Scientific), separated with sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) using the Mini-PROTEAN Tetra Cell system (Bio-Rad) and transferred to PVDF membranes (Bio-Rad).. Primary antibodies against endogenous HNF1A protein (Santa Cruz, sc-6548; 1:500), or actin (Sigma–Aldrich, A5441; 1:10000) were used, followed by HRP-conjugated secondary antibodies anti-goat IgG-HRP (Santa Cruz, sc-2354, 1:5000) and anti-mouse IgG-HRP (Bethyl labs, A90-516P, 1:10000).. Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).Chemiluminescent signals were detected using Super Signal West Dura Extended Duration substrate (Thermo Scientific).



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