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anti insulin r 309  (R&D Systems)


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    Structured Review

    R&D Systems anti insulin r 309
    Anti Insulin R 309, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti insulin r 309/product/R&D Systems
    Average 94 stars, based on 1 article reviews
    anti insulin r 309 - by Bioz Stars, 2026-05
    94/100 stars

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    Image Search Results


    Interaction and colocalization between INSR, CAV3, CAV1, and CLTC under different insulin stimulations. (A) Western blot of mice skeletal muscle lysates after insulin injection. Phospho-AKT (Ser473) to total AKT ratio or phospho-ERK1/2 to total ERK ratio was quantified ( n = 6). (B) Co-immunoprecipitation of skeletal muscle INSR after PBS or insulin injection. CLTC to INSR ratio or CAV3 to INSR ratio were quantified ( n = 7-10). (C) Representative STED microscopy images of C2C12 myoblasts expressing INSR-A-SNAP (surface labeled) that were fixed after stimulation with 0, 0.2, or 20 nM insulin for 30 minutes and stained for CAV1 and CLTC (scale bar = 5 µm). (D, E) Colocalizations between INSR-A-SNAP, CAV1, and CLTC were quantified by Object Pearson Coefficient. Data are plotted to show differences between insulin concentrations (D) or between protein pairs (E) ( n = 7-9 images, 1-4 cells per image. * P < .05, Tukey's multiple comparison after 2-ANOVA. Box represents median and 25th to 75th percentiles).

    Journal: Journal of the Endocrine Society

    Article Title: Insulin receptor trafficking and interactions in muscle cells

    doi: 10.1210/jendso/bvag020

    Figure Lengend Snippet: Interaction and colocalization between INSR, CAV3, CAV1, and CLTC under different insulin stimulations. (A) Western blot of mice skeletal muscle lysates after insulin injection. Phospho-AKT (Ser473) to total AKT ratio or phospho-ERK1/2 to total ERK ratio was quantified ( n = 6). (B) Co-immunoprecipitation of skeletal muscle INSR after PBS or insulin injection. CLTC to INSR ratio or CAV3 to INSR ratio were quantified ( n = 7-10). (C) Representative STED microscopy images of C2C12 myoblasts expressing INSR-A-SNAP (surface labeled) that were fixed after stimulation with 0, 0.2, or 20 nM insulin for 30 minutes and stained for CAV1 and CLTC (scale bar = 5 µm). (D, E) Colocalizations between INSR-A-SNAP, CAV1, and CLTC were quantified by Object Pearson Coefficient. Data are plotted to show differences between insulin concentrations (D) or between protein pairs (E) ( n = 7-9 images, 1-4 cells per image. * P < .05, Tukey's multiple comparison after 2-ANOVA. Box represents median and 25th to 75th percentiles).

    Article Snippet: INSR, CAV1, and CLTC were detected by the following Cell Signaling primary antibodies: INSRβ (1:1000, Mouse mAb, Cat. #3020S, RRID: AB_2249166), CLTC (1:1000, Rabbit mAb, Cat. #4796, RRID: AB_10828486), Caveolin-1 (1:1000, Rabbit mAb, Cat. #3267, RRID: AB_2275453), and HRP-conjugated VeriBlot secondary antibodies (1:200, anti-mouse Cat. #ab131368, RRID: AB_2895114; anti-rabbit ab131366, RRID: AB_2892718; Abcam) that do not bind to IgG heavy and light chains to reduce background noise.

    Techniques: Western Blot, Injection, Immunoprecipitation, Microscopy, Expressing, Labeling, Staining, Comparison

    Live-cell TIRF imaging of cell-surface INSR, CAV1, and CLTC. (A, B) TIRF microscopy (2 seconds/frame) showed colocalization between INSR-B-TagBFP and (A) CAV1-mRFP or (B) CLTC-mRFP. (C, D) The associated fluorescent intensity of representative INSR-B-TagBFP and colocalized (C) CAV1-mRFP or (D) CLTC-mRFP. (E-G) The (E) diffusion coefficient (μm 2 /s), (F) track radius, and (G) lifetime of INSR-B-TagBFP tracks in cells expressing CAV1-mRFP under 0 nM ( n = 2 cells, 360 tracks) or 2 nM insulin ( n = 2 cells, 324 tracks) or expressing CLTC-mRFP under 0 nM ( n = 4 cells, 917 tracks) or 2 nM insulin ( n = 2 cells, 146 tracks). Data are plotted as SuperPlot, with bigger dots showing mean values of the cells and smaller dots showing individual INSR tracks of the cells. The cumulative probability shows the distribution of the diffusion coefficient, with the dots and numbers showing the median values. (2-ANOVA: # effect of co-expression; post hoc Tukey test: * P < .05; Kolmogorov–Smirnov (KS) test: * P < .05, ** P < .005, *** P < .0005.) Experiments shown were conducted in Ringer's buffer.

    Journal: Journal of the Endocrine Society

    Article Title: Insulin receptor trafficking and interactions in muscle cells

    doi: 10.1210/jendso/bvag020

    Figure Lengend Snippet: Live-cell TIRF imaging of cell-surface INSR, CAV1, and CLTC. (A, B) TIRF microscopy (2 seconds/frame) showed colocalization between INSR-B-TagBFP and (A) CAV1-mRFP or (B) CLTC-mRFP. (C, D) The associated fluorescent intensity of representative INSR-B-TagBFP and colocalized (C) CAV1-mRFP or (D) CLTC-mRFP. (E-G) The (E) diffusion coefficient (μm 2 /s), (F) track radius, and (G) lifetime of INSR-B-TagBFP tracks in cells expressing CAV1-mRFP under 0 nM ( n = 2 cells, 360 tracks) or 2 nM insulin ( n = 2 cells, 324 tracks) or expressing CLTC-mRFP under 0 nM ( n = 4 cells, 917 tracks) or 2 nM insulin ( n = 2 cells, 146 tracks). Data are plotted as SuperPlot, with bigger dots showing mean values of the cells and smaller dots showing individual INSR tracks of the cells. The cumulative probability shows the distribution of the diffusion coefficient, with the dots and numbers showing the median values. (2-ANOVA: # effect of co-expression; post hoc Tukey test: * P < .05; Kolmogorov–Smirnov (KS) test: * P < .05, ** P < .005, *** P < .0005.) Experiments shown were conducted in Ringer's buffer.

    Article Snippet: INSR, CAV1, and CLTC were detected by the following Cell Signaling primary antibodies: INSRβ (1:1000, Mouse mAb, Cat. #3020S, RRID: AB_2249166), CLTC (1:1000, Rabbit mAb, Cat. #4796, RRID: AB_10828486), Caveolin-1 (1:1000, Rabbit mAb, Cat. #3267, RRID: AB_2275453), and HRP-conjugated VeriBlot secondary antibodies (1:200, anti-mouse Cat. #ab131368, RRID: AB_2895114; anti-rabbit ab131366, RRID: AB_2892718; Abcam) that do not bind to IgG heavy and light chains to reduce background noise.

    Techniques: Imaging, Microscopy, Diffusion-based Assay, Expressing

    Analysis of INSR tracks colocalized or not colocalized with CAV1 or CLTC. (A) INSR tracks that colocalized with CAV1 under 0 or 2 nM insulin (referred to as CAV1.Y.0nM or CAV1.Y.2nM below). (B) INSR tracks that colocalized with CLTC under 0 or 2 nM insulin (referred to as CLTC.Y.0nM or CLTC.Y.2nM below). (C) Diffusion coefficient (μm 2 /s) of INSR-B-TagBFP tracks that did not colocalize with CAV1-mRFP tracks under 0 nM insulin (CAV1.N.0nM) or 2 nM insulin (CAV1.N.2nM) or colocalized with CAV1-mRFP tracks under 0 nM insulin (CAV1.Y.0nM) or 2 nM insulin (CAV1.Y.2nM). The cumulative probability shows the distribution of the measurements, with the dots and numbers showing the median values (same for other cumulative probability plots). (D) Diffusion coefficient (μm 2 /s) of INSR-B-TagBFP tracks that did not colocalize with CLTC-mRFP tracks under 0 nM insulin (CLTC.N.0nM) or 2 nM insulin (CLTC.N.2nM) or colocalized with CLTC-mRFP tracks under 0 nM insulin (CLTC.Y.0nM) or 2 nM insulin (CLTC.Y.2nM). (E) Track radius of INSR-B-TagBFP tracks that did not colocalize with CAV1-mRFP tracks under 0 nM insulin (CAV1.N.0nM) or 2 nM insulin (CAV1.N.2nM) or colocalized with CAV1-mRFP tracks under 0 nM insulin (CAV1.Y.0nM) or 2 nM insulin (CAV1.Y.2nM). (F) Track radius of INSR-B-TagBFP tracks that did not colocalize with CLTC-mRFP tracks under 0 nM insulin (CLTC.N.0nM) or 2 nM insulin (CLTC.N.2nM) or colocalized with CLTC-mRFP tracks under 0 nM insulin (CLTC.Y.0nM) or 2 nM insulin (CLTC.Y.2nM). (G) Lifetime of INSR-B-TagBFP tracks that did not colocalize with CAV1-mRFP tracks under 0 nM insulin (CAV1.N.0nM) or 2 nM insulin (CAV1.N.2nM) or colocalized with CAV1-mRFP tracks under 0 nM insulin (CAV1.Y.0nM) or 2 nM insulin (CAV1.Y.2nM). (H) Lifetime of INSR-B-TagBFP tracks that did not colocalize with CLTC-mRFP tracks under 0 nM insulin (CLTC.N.0nM) or 2 nM insulin (CLTC.N.2nM) or colocalized with CLTC-mRFP tracks under 0 nM insulin (CLTC.Y.0nM) or 2 nM insulin (CLTC.Y.2nM). (CAV1.N.0nM, n = 2 cells, 125 tracks; CAV1.N.2 nM, n = 2 cells, 96 tracks; CAV1.Y.0nM, n = 2 cells, 235 tracks; CAV1.Y.2nM, n = 2 cells, 228 tracks; CLTC.N.0nM, n = 4 cells, 597 tracks; CLTC.N.2nM, n = 2 cells, 91 tracks; CLTC.Y.0nM, n = 4 cells, 320 tracks; CLTC.Y.2nM, n = 2 cells, 55 tracks.) (2-ANOVA: # effect of colocalization, $ effect of insulin, % interaction of the 2 variables; Kolmogorov–Smirnov [KS] test: * P < .05, *** P < .0005.) Experiments shown were conducted in Ringer's buffer.

    Journal: Journal of the Endocrine Society

    Article Title: Insulin receptor trafficking and interactions in muscle cells

    doi: 10.1210/jendso/bvag020

    Figure Lengend Snippet: Analysis of INSR tracks colocalized or not colocalized with CAV1 or CLTC. (A) INSR tracks that colocalized with CAV1 under 0 or 2 nM insulin (referred to as CAV1.Y.0nM or CAV1.Y.2nM below). (B) INSR tracks that colocalized with CLTC under 0 or 2 nM insulin (referred to as CLTC.Y.0nM or CLTC.Y.2nM below). (C) Diffusion coefficient (μm 2 /s) of INSR-B-TagBFP tracks that did not colocalize with CAV1-mRFP tracks under 0 nM insulin (CAV1.N.0nM) or 2 nM insulin (CAV1.N.2nM) or colocalized with CAV1-mRFP tracks under 0 nM insulin (CAV1.Y.0nM) or 2 nM insulin (CAV1.Y.2nM). The cumulative probability shows the distribution of the measurements, with the dots and numbers showing the median values (same for other cumulative probability plots). (D) Diffusion coefficient (μm 2 /s) of INSR-B-TagBFP tracks that did not colocalize with CLTC-mRFP tracks under 0 nM insulin (CLTC.N.0nM) or 2 nM insulin (CLTC.N.2nM) or colocalized with CLTC-mRFP tracks under 0 nM insulin (CLTC.Y.0nM) or 2 nM insulin (CLTC.Y.2nM). (E) Track radius of INSR-B-TagBFP tracks that did not colocalize with CAV1-mRFP tracks under 0 nM insulin (CAV1.N.0nM) or 2 nM insulin (CAV1.N.2nM) or colocalized with CAV1-mRFP tracks under 0 nM insulin (CAV1.Y.0nM) or 2 nM insulin (CAV1.Y.2nM). (F) Track radius of INSR-B-TagBFP tracks that did not colocalize with CLTC-mRFP tracks under 0 nM insulin (CLTC.N.0nM) or 2 nM insulin (CLTC.N.2nM) or colocalized with CLTC-mRFP tracks under 0 nM insulin (CLTC.Y.0nM) or 2 nM insulin (CLTC.Y.2nM). (G) Lifetime of INSR-B-TagBFP tracks that did not colocalize with CAV1-mRFP tracks under 0 nM insulin (CAV1.N.0nM) or 2 nM insulin (CAV1.N.2nM) or colocalized with CAV1-mRFP tracks under 0 nM insulin (CAV1.Y.0nM) or 2 nM insulin (CAV1.Y.2nM). (H) Lifetime of INSR-B-TagBFP tracks that did not colocalize with CLTC-mRFP tracks under 0 nM insulin (CLTC.N.0nM) or 2 nM insulin (CLTC.N.2nM) or colocalized with CLTC-mRFP tracks under 0 nM insulin (CLTC.Y.0nM) or 2 nM insulin (CLTC.Y.2nM). (CAV1.N.0nM, n = 2 cells, 125 tracks; CAV1.N.2 nM, n = 2 cells, 96 tracks; CAV1.Y.0nM, n = 2 cells, 235 tracks; CAV1.Y.2nM, n = 2 cells, 228 tracks; CLTC.N.0nM, n = 4 cells, 597 tracks; CLTC.N.2nM, n = 2 cells, 91 tracks; CLTC.Y.0nM, n = 4 cells, 320 tracks; CLTC.Y.2nM, n = 2 cells, 55 tracks.) (2-ANOVA: # effect of colocalization, $ effect of insulin, % interaction of the 2 variables; Kolmogorov–Smirnov [KS] test: * P < .05, *** P < .0005.) Experiments shown were conducted in Ringer's buffer.

    Article Snippet: INSR, CAV1, and CLTC were detected by the following Cell Signaling primary antibodies: INSRβ (1:1000, Mouse mAb, Cat. #3020S, RRID: AB_2249166), CLTC (1:1000, Rabbit mAb, Cat. #4796, RRID: AB_10828486), Caveolin-1 (1:1000, Rabbit mAb, Cat. #3267, RRID: AB_2275453), and HRP-conjugated VeriBlot secondary antibodies (1:200, anti-mouse Cat. #ab131368, RRID: AB_2895114; anti-rabbit ab131366, RRID: AB_2892718; Abcam) that do not bind to IgG heavy and light chains to reduce background noise.

    Techniques: Diffusion-based Assay

    Summary of the effects of CAV1 and CLTC on INSR tracks. Higher insulin (20 nM) promoted INSR and CAV1 colocalization, while lower insulin (0.2 nM) promoted INSR and CLTC colocalization. INSR tracks had lower diffusion coefficient and track radius in CAV1-overexpressing cells than CLTC-overexpressing cells. Within the same cells, INSR tracks colocalized with CAV1 had longer lifetimes and larger track radius than noncolocalized tracks. INSR tracks colocalized with CLTC had longer lifetimes than noncolocalized tracks, which is further increased by insulin.

    Journal: Journal of the Endocrine Society

    Article Title: Insulin receptor trafficking and interactions in muscle cells

    doi: 10.1210/jendso/bvag020

    Figure Lengend Snippet: Summary of the effects of CAV1 and CLTC on INSR tracks. Higher insulin (20 nM) promoted INSR and CAV1 colocalization, while lower insulin (0.2 nM) promoted INSR and CLTC colocalization. INSR tracks had lower diffusion coefficient and track radius in CAV1-overexpressing cells than CLTC-overexpressing cells. Within the same cells, INSR tracks colocalized with CAV1 had longer lifetimes and larger track radius than noncolocalized tracks. INSR tracks colocalized with CLTC had longer lifetimes than noncolocalized tracks, which is further increased by insulin.

    Article Snippet: INSR, CAV1, and CLTC were detected by the following Cell Signaling primary antibodies: INSRβ (1:1000, Mouse mAb, Cat. #3020S, RRID: AB_2249166), CLTC (1:1000, Rabbit mAb, Cat. #4796, RRID: AB_10828486), Caveolin-1 (1:1000, Rabbit mAb, Cat. #3267, RRID: AB_2275453), and HRP-conjugated VeriBlot secondary antibodies (1:200, anti-mouse Cat. #ab131368, RRID: AB_2895114; anti-rabbit ab131366, RRID: AB_2892718; Abcam) that do not bind to IgG heavy and light chains to reduce background noise.

    Techniques: Diffusion-based Assay