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rabbit polyclonal antibodies against human glut4  (Bio-Rad)


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    Structured Review

    Bio-Rad rabbit polyclonal antibodies against human glut4
    Fig. 1. In a crude membrane-enriched fraction, insulin-dependent diabetes results in no change in cardiac GLUT12 protein content, despite decreased cardiac <t>GLUT4.</t> Top panel: Western blot of cardiac muscle from healthy (Con) and type 1 diabetic (Dx) mice. Total calsequestrin (CASQ) protein content was used as a loading control. Bottom panel: Mean±SE total GLUT protein content in a crude membrane-enriched fraction, (n=5–10/group), *Pb0.05 vs. control group.
    Rabbit Polyclonal Antibodies Against Human Glut4, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 91/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal antibodies against human glut4/product/Bio-Rad
    Average 91 stars, based on 6 article reviews
    rabbit polyclonal antibodies against human glut4 - by Bioz Stars, 2026-05
    91/100 stars

    Images

    1) Product Images from "GLUT12 functions as a basal and insulin-independent glucose transporter in the heart."

    Article Title: GLUT12 functions as a basal and insulin-independent glucose transporter in the heart.

    Journal: Biochimica et biophysica acta

    doi: 10.1016/j.bbadis.2012.09.013

    Fig. 1. In a crude membrane-enriched fraction, insulin-dependent diabetes results in no change in cardiac GLUT12 protein content, despite decreased cardiac GLUT4. Top panel: Western blot of cardiac muscle from healthy (Con) and type 1 diabetic (Dx) mice. Total calsequestrin (CASQ) protein content was used as a loading control. Bottom panel: Mean±SE total GLUT protein content in a crude membrane-enriched fraction, (n=5–10/group), *Pb0.05 vs. control group.
    Figure Legend Snippet: Fig. 1. In a crude membrane-enriched fraction, insulin-dependent diabetes results in no change in cardiac GLUT12 protein content, despite decreased cardiac GLUT4. Top panel: Western blot of cardiac muscle from healthy (Con) and type 1 diabetic (Dx) mice. Total calsequestrin (CASQ) protein content was used as a loading control. Bottom panel: Mean±SE total GLUT protein content in a crude membrane-enriched fraction, (n=5–10/group), *Pb0.05 vs. control group.

    Techniques Used: Membrane, Western Blot, Control

    Fig. 4. Insulin stimulation causes significant translocation of GLUT4, but not GLUT12, to cell peripherals, as visualized by confocal laser scanning microscopy. Adult rat cardiac myocytes were incubated without (A, C) or with insulin (B, D, 100 μU/ml) for 30 min prior to immunofluorescent staining. Results were analyzed from three independent exper- iments with at least 70 cells/treatment. Scale bar: 10 μm.
    Figure Legend Snippet: Fig. 4. Insulin stimulation causes significant translocation of GLUT4, but not GLUT12, to cell peripherals, as visualized by confocal laser scanning microscopy. Adult rat cardiac myocytes were incubated without (A, C) or with insulin (B, D, 100 μU/ml) for 30 min prior to immunofluorescent staining. Results were analyzed from three independent exper- iments with at least 70 cells/treatment. Scale bar: 10 μm.

    Techniques Used: Translocation Assay, Confocal Laser Scanning Microscopy, Incubation, Staining



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    Bio-Rad rabbit polyclonal antibodies against human glut4
    Fig. 1. In a crude membrane-enriched fraction, insulin-dependent diabetes results in no change in cardiac GLUT12 protein content, despite decreased cardiac <t>GLUT4.</t> Top panel: Western blot of cardiac muscle from healthy (Con) and type 1 diabetic (Dx) mice. Total calsequestrin (CASQ) protein content was used as a loading control. Bottom panel: Mean±SE total GLUT protein content in a crude membrane-enriched fraction, (n=5–10/group), *Pb0.05 vs. control group.
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    Fig. 1. In a crude membrane-enriched fraction, insulin-dependent diabetes results in no change in cardiac GLUT12 protein content, despite decreased cardiac <t>GLUT4.</t> Top panel: Western blot of cardiac muscle from healthy (Con) and type 1 diabetic (Dx) mice. Total calsequestrin (CASQ) protein content was used as a loading control. Bottom panel: Mean±SE total GLUT protein content in a crude membrane-enriched fraction, (n=5–10/group), *Pb0.05 vs. control group.
    Rabbit Polyclonal Antibody Against Human P Lap/Irap, Glut4, Insulin Receptor, Irs 1, P Ser307 Irs1, supplied by Upstate Biotechnology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Fig. 1. In a crude membrane-enriched fraction, insulin-dependent diabetes results in no change in cardiac GLUT12 protein content, despite decreased cardiac GLUT4. Top panel: Western blot of cardiac muscle from healthy (Con) and type 1 diabetic (Dx) mice. Total calsequestrin (CASQ) protein content was used as a loading control. Bottom panel: Mean±SE total GLUT protein content in a crude membrane-enriched fraction, (n=5–10/group), *Pb0.05 vs. control group.

    Journal: Biochimica et biophysica acta

    Article Title: GLUT12 functions as a basal and insulin-independent glucose transporter in the heart.

    doi: 10.1016/j.bbadis.2012.09.013

    Figure Lengend Snippet: Fig. 1. In a crude membrane-enriched fraction, insulin-dependent diabetes results in no change in cardiac GLUT12 protein content, despite decreased cardiac GLUT4. Top panel: Western blot of cardiac muscle from healthy (Con) and type 1 diabetic (Dx) mice. Total calsequestrin (CASQ) protein content was used as a loading control. Bottom panel: Mean±SE total GLUT protein content in a crude membrane-enriched fraction, (n=5–10/group), *Pb0.05 vs. control group.

    Article Snippet: Membrane proteins were incubated with rabbit polyclonal antibodies against human GLUT4 (1:7500, AbD Serotec, Raleigh, NC) or against rat GLUT12 (1:500, Abcam, Cambridge, MA).

    Techniques: Membrane, Western Blot, Control

    Fig. 4. Insulin stimulation causes significant translocation of GLUT4, but not GLUT12, to cell peripherals, as visualized by confocal laser scanning microscopy. Adult rat cardiac myocytes were incubated without (A, C) or with insulin (B, D, 100 μU/ml) for 30 min prior to immunofluorescent staining. Results were analyzed from three independent exper- iments with at least 70 cells/treatment. Scale bar: 10 μm.

    Journal: Biochimica et biophysica acta

    Article Title: GLUT12 functions as a basal and insulin-independent glucose transporter in the heart.

    doi: 10.1016/j.bbadis.2012.09.013

    Figure Lengend Snippet: Fig. 4. Insulin stimulation causes significant translocation of GLUT4, but not GLUT12, to cell peripherals, as visualized by confocal laser scanning microscopy. Adult rat cardiac myocytes were incubated without (A, C) or with insulin (B, D, 100 μU/ml) for 30 min prior to immunofluorescent staining. Results were analyzed from three independent exper- iments with at least 70 cells/treatment. Scale bar: 10 μm.

    Article Snippet: Membrane proteins were incubated with rabbit polyclonal antibodies against human GLUT4 (1:7500, AbD Serotec, Raleigh, NC) or against rat GLUT12 (1:500, Abcam, Cambridge, MA).

    Techniques: Translocation Assay, Confocal Laser Scanning Microscopy, Incubation, Staining