trichostatin a (threefold serial dilution starting at 10 µm) served as a positive control Search Results


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Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.
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DuPont de Nemours ionomer surlyn® 1706
Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.
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Selleck Chemicals motor neurons
Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.
Motor Neurons, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Promega hdac-glotm i/ii assay
Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.
Hdac Glotm I/Ii Assay, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Fisher Scientific hat
Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.
Hat, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ONBIO Inc 4-hpr or fenritinide
Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.
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Corning Life Sciences floating nucleopore polycarbonate filter
Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.
Floating Nucleopore Polycarbonate Filter, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Drug treatments for in vitro screening
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Image Search Results


Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.

Journal: American journal of physiology. Cell physiology

Article Title: Five months of voluntary wheel running downregulates skeletal muscle LINE-1 gene expression in rats

doi: 10.1152/ajpcell.00301.2019

Figure Lengend Snippet: Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.

Article Snippet: Drug treatments for in vitro screening Treatments included AICAR (1 mM, cat. no. BML-EI330; Enzo, Farmingdale, NY), caffeine (5 mM, cat. no. A10431; Alfa Aesar, Ward Hill, MA), rotenone (100 nM, cat. no. ALX350360G001; Enzo), resveratrol (10 μM, cat. no. R0071; TCI America, Portland, OR), the global HDAC inhibitor trichostatin A (100 nM, cat. no. G656A; Promega, Madison, WI), 5-azacytidine (10 μM, TCI America), or 0.1% DMSO (cat. no. 25–950-CQC; Corning Inc., Corning, NY) as a vehicle control.

Techniques: Cell Culture, Expressing, Western Blot, Methylation, Immunoprecipitation, Methylated DNA Immunoprecipitation

Drug treatments for in vitro screening

Journal: American journal of physiology. Cell physiology

Article Title: Five months of voluntary wheel running downregulates skeletal muscle LINE-1 gene expression in rats

doi: 10.1152/ajpcell.00301.2019

Figure Lengend Snippet: Drug treatments for in vitro screening

Article Snippet: Drug treatments for in vitro screening Treatments included AICAR (1 mM, cat. no. BML-EI330; Enzo, Farmingdale, NY), caffeine (5 mM, cat. no. A10431; Alfa Aesar, Ward Hill, MA), rotenone (100 nM, cat. no. ALX350360G001; Enzo), resveratrol (10 μM, cat. no. R0071; TCI America, Portland, OR), the global HDAC inhibitor trichostatin A (100 nM, cat. no. G656A; Promega, Madison, WI), 5-azacytidine (10 μM, TCI America), or 0.1% DMSO (cat. no. 25–950-CQC; Corning Inc., Corning, NY) as a vehicle control.

Techniques: In Vitro, Concentration Assay, Activity Assay

Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.

Journal: American journal of physiology. Cell physiology

Article Title: Five months of voluntary wheel running downregulates skeletal muscle LINE-1 gene expression in rats

doi: 10.1152/ajpcell.00301.2019

Figure Lengend Snippet: Cell culture experiments to determine possible exercise-specific pathways that regulate long interspersed element-1 (L1) mRNA expression in rat L6 myotubes. A and B: mRNA expression for L1-Tot (A) and L1–3 (B) following 3-h treatments with a variety of drugs described in Table 2 (n = 4 wells/drug/vehicle treatment). C: phosphorylation of AMP-activated protein kinase (AMPK; Thr172) with increasing doses of 5-aminoimidazole-4-carboxamide ribonucleotide (AICAR) along with an accompanying Western blot representative image. D and E: effects of different AICAR doses on L1-Tot (D) and L1–3 (E) mRNA expression. F and G: L1-Tot (F) and L1–3 methylation (G) measured via methylated DNA immunoprecipitation (MeDIP). Data in A–G are presented as individual values, and all treatments were statistically compared with the DMSO control (DMSO presented as solid line at 1.0 ± SD; n = 6 wells/AICAR/vehicle treatment in C–G). 5-AZA, 5-azacytidine; CAF, caffeine; RES, resveratrol; ROT, rotenone; TA, trichostatin A. 1, 2, and 4 mM refer to the increasing concentrations of AICAR.

Article Snippet: Drug treatments for in vitro screening Treatments included AICAR (1 mM, cat. no. BML-EI330; Enzo, Farmingdale, NY), caffeine (5 mM, cat. no. A10431; Alfa Aesar, Ward Hill, MA), rotenone (100 nM, cat. no. ALX350360G001; Enzo), resveratrol (10 μM, cat. no. R0071; TCI America, Portland, OR), the global HDAC inhibitor trichostatin A (100 nM, cat. no. G656A; Promega, Madison, WI), 5-azacytidine (10 μM, TCI America), or 0.1% DMSO (cat. no. 25–950-CQC; Corning Inc., Corning, NY) as a vehicle control.

Techniques: Cell Culture, Expressing, Western Blot, Methylation, Immunoprecipitation, Methylated DNA Immunoprecipitation