scintillation liquid Search Results


tri carb liquid scintillation counter  (Revvity)
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Revvity tri carb liquid scintillation counter
Tri Carb Liquid Scintillation Counter, supplied by Revvity, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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tri carb liquid scintillation counter - by Bioz Stars, 2026-08
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liquid scintillation counter  (Revvity)
93
Revvity liquid scintillation counter
Liquid Scintillation Counter, supplied by Revvity, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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tri carb 4910 tr  (Revvity)
91
Revvity tri carb 4910 tr
Tri Carb 4910 Tr, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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tri carb 4910 tr - by Bioz Stars, 2026-08
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liquid scintillation analyzer  (Revvity)
91
Revvity liquid scintillation analyzer
PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by <t>scintillation</t> counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).
Liquid Scintillation Analyzer, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scintillation+liquid/pmc09963939-202-40-43?v=Revvity
Average 91 stars, based on 1 article reviews
liquid scintillation analyzer - by Bioz Stars, 2026-08
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cat 425 209 ecolite liquid scintillation cocktail mp biomedicals cat ic882475  (Valiant Co Ltd)
96
Valiant Co Ltd cat 425 209 ecolite liquid scintillation cocktail mp biomedicals cat ic882475
PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by <t>scintillation</t> counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).
Cat 425 209 Ecolite Liquid Scintillation Cocktail Mp Biomedicals Cat Ic882475, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cytoscint liquid scintillation cocktail  (Valiant Co Ltd)
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Valiant Co Ltd cytoscint liquid scintillation cocktail
PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by <t>scintillation</t> counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).
Cytoscint Liquid Scintillation Cocktail, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cytoscint liquid scintillation cocktail - by Bioz Stars, 2026-08
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bcs na counting scintillation 150 cocktail  (Danaher Inc)
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PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by <t>scintillation</t> counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).
Bcs Na Counting Scintillation 150 Cocktail, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ecolume liquid scintillation cocktail  (Valiant Co Ltd)
96
Valiant Co Ltd ecolume liquid scintillation cocktail
PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by <t>scintillation</t> counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).
Ecolume Liquid Scintillation Cocktail, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ecolume liquid scintillation cocktail - by Bioz Stars, 2026-08
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betamax scintillation cocktail  (Valiant Co Ltd)
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Valiant Co Ltd betamax scintillation cocktail
PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by <t>scintillation</t> counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).
Betamax Scintillation Cocktail, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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scintillation cocktail  (Valiant Co Ltd)
94
Valiant Co Ltd scintillation cocktail
PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by <t>scintillation</t> counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).
Scintillation Cocktail, supplied by Valiant 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
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maleimido ptsa para toluene sulfonic acid pdi polydispersity index phf poly  (Chem Impex International)
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Chem Impex International maleimido ptsa para toluene sulfonic acid pdi polydispersity index phf poly
PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by <t>scintillation</t> counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).
Maleimido Ptsa Para Toluene Sulfonic Acid Pdi Polydispersity Index Phf Poly, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by scintillation counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).

Journal: International Journal of Molecular Sciences

Article Title: Acute PDE4 Inhibition Induces a Transient Increase in Blood Glucose in Mice

doi: 10.3390/ijms24043260

Figure Lengend Snippet: PDE4 inhibition induces glycogenolysis in skeletal muscle and inhibits glucose uptake in skeletal muscle and heart. ( A ) PDE4 inhibition induces glycogenolysis in skeletal muscle. The glycogen levels in the liver and skeletal muscle (gastrocnemius) in postprandial mice are shown after treatment with the PAN-PDE4 inhibitor roflumilast (Rofl; 5 mg/kg; i.p.) or solvent control (Solv) for 90 min. Data are expressed as mg of glycogen per g of tissue weight. ( B ) PAN-PDE4 inhibition reduces locomotion, as reflected by reduced travel distance. Mice were injected with the PDE4 inhibitor rolipram (3 mg/kg; i.p.; n = 6) or solvent control, placed immediately in a new cage, and then locomotion was assessed using SmartCageTM technology. Traces represent changes in travel distance (cm per 5 min interval). ( C ) Postprandial mice were injected with the PDE4 inhibitor roflumilast (5 mg/kg; i.p.) or solvent control, followed 15 min later by injection with [ 3 H]-2-deoxyglucose (intravenous, i.v.). Animals were euthanized 30 min after the tracer injection, their tissues were homogenized, and the phosphorylated [ 3 H]-2-deoxyglucose-6-phosphate was isolated by anion exchange chromatography and quantified by scintillation counting. Data are expressed as pmol [ 3 H]-2-deoxyglucose-6-phosphate per g of tissue wet weight. All data represent the mean ± SEM. Statistical significance was determined using the Mann–Whitney test (bar graphs) or a two-way ANOVA with Sidak’s post hoc test (time courses) and is indicated as ns ( p > 0.05), * ( p < 0.05), and ** ( p < 0.01).

Article Snippet: After washing the columns twice with 1 mL of deionized water, the [ 3 H]-2-deoxyglucose-6-phosphate was eluted from the columns using 2 × 1 ml of 1.5 M NaCl, and the radioactivity in the eluates was then quantified using a liquid scintillation analyzer (PerkinElmer Tri-Carb ® 4810 TR).

Techniques: Inhibition, Solvent, Control, Injection, Isolation, Chromatography, MANN-WHITNEY