cell culture rat l6 skeletal muscle cell line Search Results


90
National Centre for Cell Science l6 rat skeletal muscle cells
L6 Rat Skeletal Muscle Cells, supplied by National Centre for Cell Science, 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/result/l6 rat skeletal muscle cells/product/National Centre for Cell Science
Average 90 stars, based on 1 article reviews
l6 rat skeletal muscle cells - by Bioz Stars, 2026-03
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90
Korean Cell Line Bank rat skeletal muscle cell line l6
Rat Skeletal Muscle Cell Line L6, supplied by Korean Cell Line Bank, 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/result/rat skeletal muscle cell line l6/product/Korean Cell Line Bank
Average 90 stars, based on 1 article reviews
rat skeletal muscle cell line l6 - by Bioz Stars, 2026-03
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90
National Centre for Cell Science rat skeletal myoblast (l6) cell line
Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the tyrosine phosphorylation of insulin receptor substrate 1 (IRS-1) in <t>L6</t> <t>myoblast</t> derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min).†p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test
Rat Skeletal Myoblast (L6) Cell Line, supplied by National Centre for Cell Science, 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/result/rat skeletal myoblast (l6) cell line/product/National Centre for Cell Science
Average 90 stars, based on 1 article reviews
rat skeletal myoblast (l6) cell line - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

90
NanoLive Inc mitochondria from rat l6 skeletal muscle cell (shown in red)
Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the tyrosine phosphorylation of insulin receptor substrate 1 (IRS-1) in <t>L6</t> <t>myoblast</t> derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min).†p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test
Mitochondria From Rat L6 Skeletal Muscle Cell (Shown In Red), supplied by NanoLive Inc, 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/result/mitochondria from rat l6 skeletal muscle cell (shown in red)/product/NanoLive Inc
Average 90 stars, based on 1 article reviews
mitochondria from rat l6 skeletal muscle cell (shown in red) - by Bioz Stars, 2026-03
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European Collection of Authenticated Cell Cultures rat skeletal muscle myoblast cell line l6.c11
Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the tyrosine phosphorylation of insulin receptor substrate 1 (IRS-1) in <t>L6</t> <t>myoblast</t> derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min).†p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test
Rat Skeletal Muscle Myoblast Cell Line L6.C11, supplied by European Collection of Authenticated Cell Cultures, 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/result/rat skeletal muscle myoblast cell line l6.c11/product/European Collection of Authenticated Cell Cultures
Average 90 stars, based on 1 article reviews
rat skeletal muscle myoblast cell line l6.c11 - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the tyrosine phosphorylation of insulin receptor substrate 1 (IRS-1) in L6 myoblast derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min).†p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test

Journal: Journal of Diabetes and Metabolic Disorders

Article Title: Effect of sub-toxic chlorpyrifos on redox sensitive kinases and insulin signaling in rat L6 myotubes

doi: 10.1007/s40200-018-0379-x

Figure Lengend Snippet: Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the tyrosine phosphorylation of insulin receptor substrate 1 (IRS-1) in L6 myoblast derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min).†p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test

Article Snippet: Rat skeletal myoblast (L6) cell line was obtained from the National Centre for Cell Sciences (Pune, India) and propagated at 37 °C in 5% CO 2 incubator in DMEM supplemented with 100 units/ml of penicillin G, 100 μg/ml of streptomycin sulfate, 0.25 μg/ml amphotericin B and 10% FBS.

Techniques: Phospho-proteomics, Derivative Assay, Western Blot, Hybridization, Control, Comparison

Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the serine phosphorylation of Akt in L6 myoblast derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min). †p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test

Journal: Journal of Diabetes and Metabolic Disorders

Article Title: Effect of sub-toxic chlorpyrifos on redox sensitive kinases and insulin signaling in rat L6 myotubes

doi: 10.1007/s40200-018-0379-x

Figure Lengend Snippet: Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the serine phosphorylation of Akt in L6 myoblast derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min). †p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test

Article Snippet: Rat skeletal myoblast (L6) cell line was obtained from the National Centre for Cell Sciences (Pune, India) and propagated at 37 °C in 5% CO 2 incubator in DMEM supplemented with 100 units/ml of penicillin G, 100 μg/ml of streptomycin sulfate, 0.25 μg/ml amphotericin B and 10% FBS.

Techniques: Phospho-proteomics, Derivative Assay, Western Blot, Hybridization, Control, Comparison

Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the phosphorylation of p38 MAPK in L6 myoblast derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min). †p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test

Journal: Journal of Diabetes and Metabolic Disorders

Article Title: Effect of sub-toxic chlorpyrifos on redox sensitive kinases and insulin signaling in rat L6 myotubes

doi: 10.1007/s40200-018-0379-x

Figure Lengend Snippet: Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the phosphorylation of p38 MAPK in L6 myoblast derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min). †p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test

Article Snippet: Rat skeletal myoblast (L6) cell line was obtained from the National Centre for Cell Sciences (Pune, India) and propagated at 37 °C in 5% CO 2 incubator in DMEM supplemented with 100 units/ml of penicillin G, 100 μg/ml of streptomycin sulfate, 0.25 μg/ml amphotericin B and 10% FBS.

Techniques: Phospho-proteomics, Derivative Assay, Western Blot, Hybridization, Control, Comparison

Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the phosphorylation of IκBα in L6 myoblast derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min). †p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test

Journal: Journal of Diabetes and Metabolic Disorders

Article Title: Effect of sub-toxic chlorpyrifos on redox sensitive kinases and insulin signaling in rat L6 myotubes

doi: 10.1007/s40200-018-0379-x

Figure Lengend Snippet: Bar diagram showing the effect of Chlorpyrifos exposure for 18hrs on the phosphorylation of IκBα in L6 myoblast derived myotubes after normalized with beta actin by western blot hybridization. Data shown are means with standard errors of three independent experiments. C+i = Control with insulin, CPF6+i = Chlorpyrifos (6mg/L) exposure for 18 hrs followed by treatment with insulin (1uM for 20min), CPF12+i = Chlorpyrifos 12mg/L exposure for 18hrs followed by treatment with insulin (1uM for 20min). †p<0.05 in comparison to control, *p<0.05 in comparison to Chlorpyrifos 6mg/L exposure groups by one way ANOVA followed by Tukey HSD post-hoc test

Article Snippet: Rat skeletal myoblast (L6) cell line was obtained from the National Centre for Cell Sciences (Pune, India) and propagated at 37 °C in 5% CO 2 incubator in DMEM supplemented with 100 units/ml of penicillin G, 100 μg/ml of streptomycin sulfate, 0.25 μg/ml amphotericin B and 10% FBS.

Techniques: Phospho-proteomics, Derivative Assay, Western Blot, Hybridization, Control, Comparison