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rabbit primary antibody against glut4  (ABclonal Biotechnology)


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    Structured Review

    ABclonal Biotechnology rabbit primary antibody against glut4
    Rabbit Primary Antibody Against Glut4, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+primary+antibody+against+glut4/glut4+antibody/pm37667357-72-45-51
    Average 90 stars, based on 1 article reviews
    rabbit primary antibody against glut4 - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Incubation:

    Article Title: Perilipin 5 deficiency aggravates cardiac hypertrophy by stimulating lactate production in leptin-deficient mice.
    Article Snippet: .. After treatment with 100 μM OA and 100 μM PA for 24 h, the cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100 for 10 min. After being blocked with 10% normal goat serum in PBS, the cells were incubated with a rabbit primary antibody against GLUT4 (1:200) (Abclonal) overnight at 4 °C. .. This step was followed by incubation with a fluorochrome-conjugated secondary donkey anti-rabbit antibody for 1 h in the dark (Invitrogen).

    Article Title: Perilipin 5 deficiency aggravates cardiac hypertrophy by stimulating lactate production in leptin-deficient mice
    Article Snippet: .. After treatment with 100 μM OA and 100 μM PA for 24 h, the cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100 for 10 min. After being blocked with 10% normal goat serum in PBS, the cells were incubated with a rabbit primary antibody against GLUT4 (1:200) (Abclonal) overnight at 4 °C. .. This step was followed by incubation with a fluorochrome-conjugated secondary donkey anti-rabbit antibody for 1 h in the dark (Invitrogen).



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    Thermo Fisher primary antibody raised against glut4 (rabbit polyclonal; no. pa5-23052; lot wj3403509
    a , Graphical representation of the EHC. b , GIR during the insulin clamp. c – e , GIR ( c ), endogenous glucose rate of appearance (RA) ( d ) and glucose rate of disappearance (RD) ( e ) at 120 min of the clamp. f , Plasma FAs during the clamp. g , Average leg glucose uptake during the last 40 min of the clamp. h , Targeted immunoblotting analyses of proteins associated with glucose metabolism, fat metabolism and the mitochondrial electron transport chain in skeletal muscle. i , Volcano plot showing proteome log 2 fold change (FC) (carriers/controls) plotted against –log 10 P value highlighting downregulated proteins TBC1D4, TBC1D1 and <t>GLUT4</t> (SLC2A4). *Difference between TBC1D4 carriers and controls at the given time point. ‡Different from basal (time 0) within the same group. n = 5 ( b – g , i ). n = 7 ( h ) except for mTOR, p70S6K and ACC ( n = 5 in controls and TBC1D4 carriers) as well as Akt2, AMPKα2, CS, CD36 and FATP4 ( n = 6) in controls and GLUT1 ( n = 6) in TBC1D4 carriers. Data are means ± s.e.m. Data were analysed using a two-tailed paired Student’s t -test ( c – e , g ), a two-tailed non-paired Student’s t -test ( h ) as well as a two-way repeated ANOVA test (two-factor repeated) and two-tailed Student–Newman–Keuls post hoc analyses for multiple comparisons ( b , f ). Graphics in a created using BioRender.com . a.u., arbitrary units.
    Primary Antibody Raised Against Glut4 (Rabbit Polyclonal; No. Pa5 23052; Lot Wj3403509, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+primary+antibody+against+glut4/pmc11659169-238-43-50
    Average 90 stars, based on 1 article reviews
    primary antibody raised against glut4 (rabbit polyclonal; no. pa5-23052; lot wj3403509 - by Bioz Stars, 2026-09
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    ABclonal Biotechnology rabbit primary antibody against glut4
    a , Graphical representation of the EHC. b , GIR during the insulin clamp. c – e , GIR ( c ), endogenous glucose rate of appearance (RA) ( d ) and glucose rate of disappearance (RD) ( e ) at 120 min of the clamp. f , Plasma FAs during the clamp. g , Average leg glucose uptake during the last 40 min of the clamp. h , Targeted immunoblotting analyses of proteins associated with glucose metabolism, fat metabolism and the mitochondrial electron transport chain in skeletal muscle. i , Volcano plot showing proteome log 2 fold change (FC) (carriers/controls) plotted against –log 10 P value highlighting downregulated proteins TBC1D4, TBC1D1 and <t>GLUT4</t> (SLC2A4). *Difference between TBC1D4 carriers and controls at the given time point. ‡Different from basal (time 0) within the same group. n = 5 ( b – g , i ). n = 7 ( h ) except for mTOR, p70S6K and ACC ( n = 5 in controls and TBC1D4 carriers) as well as Akt2, AMPKα2, CS, CD36 and FATP4 ( n = 6) in controls and GLUT1 ( n = 6) in TBC1D4 carriers. Data are means ± s.e.m. Data were analysed using a two-tailed paired Student’s t -test ( c – e , g ), a two-tailed non-paired Student’s t -test ( h ) as well as a two-way repeated ANOVA test (two-factor repeated) and two-tailed Student–Newman–Keuls post hoc analyses for multiple comparisons ( b , f ). Graphics in a created using BioRender.com . a.u., arbitrary units.
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    Average 90 stars, based on 1 article reviews
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    Merck KGaA primary rabbit antibody against glut4
    a , Graphical representation of the EHC. b , GIR during the insulin clamp. c – e , GIR ( c ), endogenous glucose rate of appearance (RA) ( d ) and glucose rate of disappearance (RD) ( e ) at 120 min of the clamp. f , Plasma FAs during the clamp. g , Average leg glucose uptake during the last 40 min of the clamp. h , Targeted immunoblotting analyses of proteins associated with glucose metabolism, fat metabolism and the mitochondrial electron transport chain in skeletal muscle. i , Volcano plot showing proteome log 2 fold change (FC) (carriers/controls) plotted against –log 10 P value highlighting downregulated proteins TBC1D4, TBC1D1 and <t>GLUT4</t> (SLC2A4). *Difference between TBC1D4 carriers and controls at the given time point. ‡Different from basal (time 0) within the same group. n = 5 ( b – g , i ). n = 7 ( h ) except for mTOR, p70S6K and ACC ( n = 5 in controls and TBC1D4 carriers) as well as Akt2, AMPKα2, CS, CD36 and FATP4 ( n = 6) in controls and GLUT1 ( n = 6) in TBC1D4 carriers. Data are means ± s.e.m. Data were analysed using a two-tailed paired Student’s t -test ( c – e , g ), a two-tailed non-paired Student’s t -test ( h ) as well as a two-way repeated ANOVA test (two-factor repeated) and two-tailed Student–Newman–Keuls post hoc analyses for multiple comparisons ( b , f ). Graphics in a created using BioRender.com . a.u., arbitrary units.
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    Becton Dickinson primary rabbit antibodies against glut4
    a , Graphical representation of the EHC. b , GIR during the insulin clamp. c – e , GIR ( c ), endogenous glucose rate of appearance (RA) ( d ) and glucose rate of disappearance (RD) ( e ) at 120 min of the clamp. f , Plasma FAs during the clamp. g , Average leg glucose uptake during the last 40 min of the clamp. h , Targeted immunoblotting analyses of proteins associated with glucose metabolism, fat metabolism and the mitochondrial electron transport chain in skeletal muscle. i , Volcano plot showing proteome log 2 fold change (FC) (carriers/controls) plotted against –log 10 P value highlighting downregulated proteins TBC1D4, TBC1D1 and <t>GLUT4</t> (SLC2A4). *Difference between TBC1D4 carriers and controls at the given time point. ‡Different from basal (time 0) within the same group. n = 5 ( b – g , i ). n = 7 ( h ) except for mTOR, p70S6K and ACC ( n = 5 in controls and TBC1D4 carriers) as well as Akt2, AMPKα2, CS, CD36 and FATP4 ( n = 6) in controls and GLUT1 ( n = 6) in TBC1D4 carriers. Data are means ± s.e.m. Data were analysed using a two-tailed paired Student’s t -test ( c – e , g ), a two-tailed non-paired Student’s t -test ( h ) as well as a two-way repeated ANOVA test (two-factor repeated) and two-tailed Student–Newman–Keuls post hoc analyses for multiple comparisons ( b , f ). Graphics in a created using BioRender.com . a.u., arbitrary units.
    Primary Rabbit Antibodies Against Glut4, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+primary+antibody+against+glut4/hif+1%CE%B1+antibody/pm20599739-38-25-29
    Average 90 stars, based on 1 article reviews
    primary rabbit antibodies against glut4 - by Bioz Stars, 2026-09
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    Image Search Results


    a , Graphical representation of the EHC. b , GIR during the insulin clamp. c – e , GIR ( c ), endogenous glucose rate of appearance (RA) ( d ) and glucose rate of disappearance (RD) ( e ) at 120 min of the clamp. f , Plasma FAs during the clamp. g , Average leg glucose uptake during the last 40 min of the clamp. h , Targeted immunoblotting analyses of proteins associated with glucose metabolism, fat metabolism and the mitochondrial electron transport chain in skeletal muscle. i , Volcano plot showing proteome log 2 fold change (FC) (carriers/controls) plotted against –log 10 P value highlighting downregulated proteins TBC1D4, TBC1D1 and GLUT4 (SLC2A4). *Difference between TBC1D4 carriers and controls at the given time point. ‡Different from basal (time 0) within the same group. n = 5 ( b – g , i ). n = 7 ( h ) except for mTOR, p70S6K and ACC ( n = 5 in controls and TBC1D4 carriers) as well as Akt2, AMPKα2, CS, CD36 and FATP4 ( n = 6) in controls and GLUT1 ( n = 6) in TBC1D4 carriers. Data are means ± s.e.m. Data were analysed using a two-tailed paired Student’s t -test ( c – e , g ), a two-tailed non-paired Student’s t -test ( h ) as well as a two-way repeated ANOVA test (two-factor repeated) and two-tailed Student–Newman–Keuls post hoc analyses for multiple comparisons ( b , f ). Graphics in a created using BioRender.com . a.u., arbitrary units.

    Journal: Nature Metabolism

    Article Title: Skeletal muscle from TBC1D4 p.Arg684Ter variant carriers is severely insulin resistant but exhibits normal metabolic responses during exercise

    doi: 10.1038/s42255-024-01153-1

    Figure Lengend Snippet: a , Graphical representation of the EHC. b , GIR during the insulin clamp. c – e , GIR ( c ), endogenous glucose rate of appearance (RA) ( d ) and glucose rate of disappearance (RD) ( e ) at 120 min of the clamp. f , Plasma FAs during the clamp. g , Average leg glucose uptake during the last 40 min of the clamp. h , Targeted immunoblotting analyses of proteins associated with glucose metabolism, fat metabolism and the mitochondrial electron transport chain in skeletal muscle. i , Volcano plot showing proteome log 2 fold change (FC) (carriers/controls) plotted against –log 10 P value highlighting downregulated proteins TBC1D4, TBC1D1 and GLUT4 (SLC2A4). *Difference between TBC1D4 carriers and controls at the given time point. ‡Different from basal (time 0) within the same group. n = 5 ( b – g , i ). n = 7 ( h ) except for mTOR, p70S6K and ACC ( n = 5 in controls and TBC1D4 carriers) as well as Akt2, AMPKα2, CS, CD36 and FATP4 ( n = 6) in controls and GLUT1 ( n = 6) in TBC1D4 carriers. Data are means ± s.e.m. Data were analysed using a two-tailed paired Student’s t -test ( c – e , g ), a two-tailed non-paired Student’s t -test ( h ) as well as a two-way repeated ANOVA test (two-factor repeated) and two-tailed Student–Newman–Keuls post hoc analyses for multiple comparisons ( b , f ). Graphics in a created using BioRender.com . a.u., arbitrary units.

    Article Snippet: For staining, four to six individual fibres were teased out from the fixed fibre bundles with fine forceps and blocked for 2 h in PBS containing 5% goat serum, 1% BSA and 0.04% saponin and then incubated overnight with primary antibody raised against GLUT4 (rabbit polyclonal; no. PA5-23052; lot WJ3403509, Thermo Scientific).

    Techniques: Western Blot, Two Tailed Test

    a , Representative immunoblots for data related to figure panel 2 h. b , c , Distribution of Myosin Heavy Chains (MHC) ( b ) and regulatory metabolic ( c ) proteins in MHC-defined type 1 and type 2 skeletal muscle fiber bundles. d , Representative immunoblots. e , Quantification of GLUT4 imaging by confocal microscopy of isolated skeletal muscle fibers. n = 7 in Controls and n = 6 in TBC1D4 carriers ( b , c ). n = 15 fibers obtained from 3 subjects (4 to 6 fibers/subject) in each group ( e ). Data are means ± SEM. Data were analyzed using a two-tailed non-paired students t-test ( e ) as well as a two-way repeated ANOVA test (one factor repeated) and two-tailed Student-Newman-Keuls post hoc analyses for multiple comparisons ( b , c ). AU, arbitrary units. Scale bar in panel e is 10 µm.

    Journal: Nature Metabolism

    Article Title: Skeletal muscle from TBC1D4 p.Arg684Ter variant carriers is severely insulin resistant but exhibits normal metabolic responses during exercise

    doi: 10.1038/s42255-024-01153-1

    Figure Lengend Snippet: a , Representative immunoblots for data related to figure panel 2 h. b , c , Distribution of Myosin Heavy Chains (MHC) ( b ) and regulatory metabolic ( c ) proteins in MHC-defined type 1 and type 2 skeletal muscle fiber bundles. d , Representative immunoblots. e , Quantification of GLUT4 imaging by confocal microscopy of isolated skeletal muscle fibers. n = 7 in Controls and n = 6 in TBC1D4 carriers ( b , c ). n = 15 fibers obtained from 3 subjects (4 to 6 fibers/subject) in each group ( e ). Data are means ± SEM. Data were analyzed using a two-tailed non-paired students t-test ( e ) as well as a two-way repeated ANOVA test (one factor repeated) and two-tailed Student-Newman-Keuls post hoc analyses for multiple comparisons ( b , c ). AU, arbitrary units. Scale bar in panel e is 10 µm.

    Article Snippet: For staining, four to six individual fibres were teased out from the fixed fibre bundles with fine forceps and blocked for 2 h in PBS containing 5% goat serum, 1% BSA and 0.04% saponin and then incubated overnight with primary antibody raised against GLUT4 (rabbit polyclonal; no. PA5-23052; lot WJ3403509, Thermo Scientific).

    Techniques: Western Blot, Imaging, Confocal Microscopy, Isolation, Two Tailed Test