glut-4 protein Search Results


glut4 primary antibody  (Boster Bio)
93
Boster Bio glut4 primary antibody
Glut4 Primary Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/glut-4+protein/Anti-ASPSCR1%2FTug+Antibody/pmc09281957-58-0-6
Average 93 stars, based on 1 article reviews
glut4 primary antibody - by Bioz Stars, 2026-09
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anti glut4 primary antibody  (Boster Bio)
90
Boster Bio anti glut4 primary antibody
Anti Glut4 Primary Antibody, supplied by Boster Bio, 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/glut-4+protein/Anti-HDBP1+Antibody/pm35844917-53-0-7
Average 90 stars, based on 1 article reviews
anti glut4 primary antibody - by Bioz Stars, 2026-09
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l6 cell line overexpressing glut4 with a myc protein tag (glut4-myc)  (AstraZeneca ltd)
90
AstraZeneca ltd l6 cell line overexpressing glut4 with a myc protein tag (glut4-myc)
L6 Cell Line Overexpressing Glut4 With A Myc Protein Tag (Glut4 Myc), supplied by AstraZeneca ltd, 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/glut-4+protein/l6+cell+line+overexpressing+glut4+with+a+myc+protein+tag++glut4+myc+/pmc04187550-83-27-17
Average 90 stars, based on 1 article reviews
l6 cell line overexpressing glut4 with a myc protein tag (glut4-myc) - by Bioz Stars, 2026-09
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rat l6 glut4-myc skeletal muscle cells expressing c-myc–tagged glut4 protein  (Absolute Biotech)
90
Absolute Biotech rat l6 glut4-myc skeletal muscle cells expressing c-myc–tagged glut4 protein
N-WASP inhibition blunts insulin-stimulated glucose uptake and <t>GLUT4</t> translocation. A, L6-GLUT4myc myoblasts were treated with vehicle (DMSO) or 10 μm WISK and stimulated with 100 nm insulin for 20 min simultaneously. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. **, p < 0.01. B, L6-GLUT4myc myoblasts were treated with 0, 5, 10, 20, or 25 μm WISK together with 100 nm insulin for a total of 20 min. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. ***, p < 0.001. C, L6-GLUT4myc myotubes were used for 2-deoxyglucose uptake assays. Values are means ± S.D. from three independent sets of cells. *, p < 0.05. D and E, L6-GLUT4myc myoblasts were treated with DMSO or WISK, and the cellular ATP levels and percentage of viable cells were determined, respectively. Values are means ± S.D. from three independent sets of cells. **, p < 0.01; ***, p < 0.001.
Rat L6 Glut4 Myc Skeletal Muscle Cells Expressing C Myc–Tagged Glut4 Protein, supplied by Absolute Biotech, 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/glut-4+protein/rat+l6+glut4+myc+skeletal+muscle+cells+expressing+c+myc+tagged+glut4+protein/pmc05704484-264-9-14
Average 90 stars, based on 1 article reviews
rat l6 glut4-myc skeletal muscle cells expressing c-myc–tagged glut4 protein - by Bioz Stars, 2026-09
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insulin-stimulated glut4 protein translocation  (Kettenbach GmbH)
90
Kettenbach GmbH insulin-stimulated glut4 protein translocation
N-WASP inhibition blunts insulin-stimulated glucose uptake and <t>GLUT4</t> translocation. A, L6-GLUT4myc myoblasts were treated with vehicle (DMSO) or 10 μm WISK and stimulated with 100 nm insulin for 20 min simultaneously. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. **, p < 0.01. B, L6-GLUT4myc myoblasts were treated with 0, 5, 10, 20, or 25 μm WISK together with 100 nm insulin for a total of 20 min. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. ***, p < 0.001. C, L6-GLUT4myc myotubes were used for 2-deoxyglucose uptake assays. Values are means ± S.D. from three independent sets of cells. *, p < 0.05. D and E, L6-GLUT4myc myoblasts were treated with DMSO or WISK, and the cellular ATP levels and percentage of viable cells were determined, respectively. Values are means ± S.D. from three independent sets of cells. **, p < 0.01; ***, p < 0.001.
Insulin Stimulated Glut4 Protein Translocation, supplied by Kettenbach GmbH, 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/glut-4+protein/insulin+stimulated+glut4+protein+translocation/10__1021_slash_acs__jmedchem__1c00410-664-19-9
Average 90 stars, based on 1 article reviews
insulin-stimulated glut4 protein translocation - by Bioz Stars, 2026-09
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nogo a  (Shanghai Korain Biotech Co Ltd)
94
Shanghai Korain Biotech Co Ltd nogo a
N-WASP inhibition blunts insulin-stimulated glucose uptake and <t>GLUT4</t> translocation. A, L6-GLUT4myc myoblasts were treated with vehicle (DMSO) or 10 μm WISK and stimulated with 100 nm insulin for 20 min simultaneously. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. **, p < 0.01. B, L6-GLUT4myc myoblasts were treated with 0, 5, 10, 20, or 25 μm WISK together with 100 nm insulin for a total of 20 min. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. ***, p < 0.001. C, L6-GLUT4myc myotubes were used for 2-deoxyglucose uptake assays. Values are means ± S.D. from three independent sets of cells. *, p < 0.05. D and E, L6-GLUT4myc myoblasts were treated with DMSO or WISK, and the cellular ATP levels and percentage of viable cells were determined, respectively. Values are means ± S.D. from three independent sets of cells. **, p < 0.01; ***, p < 0.001.
Nogo A, supplied by Shanghai Korain Biotech Co Ltd, 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/product/glut-4+protein/Rat+Reticulon+4/pm41318073-46-8-21
Average 94 stars, based on 1 article reviews
nogo a - by Bioz Stars, 2026-09
94/100 stars
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glut4 protein  (The Company of Biologists)
90
The Company of Biologists glut4 protein
N-WASP inhibition blunts insulin-stimulated glucose uptake and <t>GLUT4</t> translocation. A, L6-GLUT4myc myoblasts were treated with vehicle (DMSO) or 10 μm WISK and stimulated with 100 nm insulin for 20 min simultaneously. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. **, p < 0.01. B, L6-GLUT4myc myoblasts were treated with 0, 5, 10, 20, or 25 μm WISK together with 100 nm insulin for a total of 20 min. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. ***, p < 0.001. C, L6-GLUT4myc myotubes were used for 2-deoxyglucose uptake assays. Values are means ± S.D. from three independent sets of cells. *, p < 0.05. D and E, L6-GLUT4myc myoblasts were treated with DMSO or WISK, and the cellular ATP levels and percentage of viable cells were determined, respectively. Values are means ± S.D. from three independent sets of cells. **, p < 0.01; ***, p < 0.001.
Glut4 Protein, supplied by The Company of Biologists, 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/glut-4+protein/glut4+protein/pm09004032-14-15-12
Average 90 stars, based on 1 article reviews
glut4 protein - by Bioz Stars, 2026-09
90/100 stars
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glut4 protein  (Federation of European Neuroscience Societies)
90
Federation of European Neuroscience Societies glut4 protein
N-WASP inhibition blunts insulin-stimulated glucose uptake and <t>GLUT4</t> translocation. A, L6-GLUT4myc myoblasts were treated with vehicle (DMSO) or 10 μm WISK and stimulated with 100 nm insulin for 20 min simultaneously. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. **, p < 0.01. B, L6-GLUT4myc myoblasts were treated with 0, 5, 10, 20, or 25 μm WISK together with 100 nm insulin for a total of 20 min. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. ***, p < 0.001. C, L6-GLUT4myc myotubes were used for 2-deoxyglucose uptake assays. Values are means ± S.D. from three independent sets of cells. *, p < 0.05. D and E, L6-GLUT4myc myoblasts were treated with DMSO or WISK, and the cellular ATP levels and percentage of viable cells were determined, respectively. Values are means ± S.D. from three independent sets of cells. **, p < 0.01; ***, p < 0.001.
Glut4 Protein, supplied by Federation of European Neuroscience Societies, 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/glut-4+protein/snare+proteins+involved+in+the+late+steps+of+glut4+translocation/pm10544260-4-39-42
Average 90 stars, based on 1 article reviews
glut4 protein - by Bioz Stars, 2026-09
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recombinant human glut4 gst (n-term) protein  (Novus Biologicals)
N/A
Recombinant Human Glut4 GST (N-Term) Protein
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recombinant human glut4 protein  (Novus Biologicals)
N/A
The Recombinant Human Glut4 Protein has been validated for the following applications Western Blot ELISA Protein Array Immunoaffinity Purification
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N-WASP inhibition blunts insulin-stimulated glucose uptake and GLUT4 translocation. A, L6-GLUT4myc myoblasts were treated with vehicle (DMSO) or 10 μm WISK and stimulated with 100 nm insulin for 20 min simultaneously. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. **, p < 0.01. B, L6-GLUT4myc myoblasts were treated with 0, 5, 10, 20, or 25 μm WISK together with 100 nm insulin for a total of 20 min. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. ***, p < 0.001. C, L6-GLUT4myc myotubes were used for 2-deoxyglucose uptake assays. Values are means ± S.D. from three independent sets of cells. *, p < 0.05. D and E, L6-GLUT4myc myoblasts were treated with DMSO or WISK, and the cellular ATP levels and percentage of viable cells were determined, respectively. Values are means ± S.D. from three independent sets of cells. **, p < 0.01; ***, p < 0.001.

Journal: The Journal of Biological Chemistry

Article Title: The actin-related p41ARC subunit contributes to p21-activated kinase-1 (PAK1)–mediated glucose uptake into skeletal muscle cells

doi: 10.1074/jbc.M117.801340

Figure Lengend Snippet: N-WASP inhibition blunts insulin-stimulated glucose uptake and GLUT4 translocation. A, L6-GLUT4myc myoblasts were treated with vehicle (DMSO) or 10 μm WISK and stimulated with 100 nm insulin for 20 min simultaneously. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. **, p < 0.01. B, L6-GLUT4myc myoblasts were treated with 0, 5, 10, 20, or 25 μm WISK together with 100 nm insulin for a total of 20 min. Cells were fixed and left unpermeabilized for labeling with anti-myc antibody. The immunofluorescent intensity of cell surface GLUT4 was normalized to the nucleic acid staining dye Syto 60. Values are means ± S.D. from three independent sets of cells. ***, p < 0.001. C, L6-GLUT4myc myotubes were used for 2-deoxyglucose uptake assays. Values are means ± S.D. from three independent sets of cells. *, p < 0.05. D and E, L6-GLUT4myc myoblasts were treated with DMSO or WISK, and the cellular ATP levels and percentage of viable cells were determined, respectively. Values are means ± S.D. from three independent sets of cells. **, p < 0.01; ***, p < 0.001.

Article Snippet: Materials Rat L6 GLUT4-myc skeletal muscle cells expressing c-myc–tagged GLUT4 protein were purchased from Kerafast and cultured as described previously ( 48 ).

Techniques: Inhibition, Translocation Assay, Labeling, Staining