cntf chemicals, peptides, and recombinant proteins Search Results


97
R&D Systems tgf beta 1
Tgf Beta 1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Selleck Chemicals peptides
Peptides, supplied by Selleck Chemicals, 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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Bio X Cell be0003 1 rrid ab 1107636 chemicals peptides
Be0003 1 Rrid Ab 1107636 Chemicals Peptides, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad protein assay dye reagent concentrate bio rad 5000006 chemical compound
Protein Assay Dye Reagent Concentrate Bio Rad 5000006 Chemical Compound, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Proteintech cl488 66240 rrid ab 2883292 biological samples paraffin embedded human lung adc specimens nyu langone health n a chemicals peptides
Cl488 66240 Rrid Ab 2883292 Biological Samples Paraffin Embedded Human Lung Adc Specimens Nyu Langone Health N A Chemicals Peptides, supplied by Proteintech, 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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Selleck Chemicals rgds
Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative <t>control</t> <t>RGD</t> (Con) or <t>RGDS</t> (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.
Rgds, supplied by Selleck Chemicals, 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/cntf+chemicals%2C+peptides%2C+and+recombinant+proteins/RGD+(Arg-Gly-Asp)+Peptides/pm39187065-49-29-31
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Gold Biotechnology Inc recombinant proteins nourseothricin goldbio n 500 calcofluor white stain sigma aldrich
Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative <t>control</t> <t>RGD</t> (Con) or <t>RGDS</t> (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.
Recombinant Proteins Nourseothricin Goldbio N 500 Calcofluor White Stain Sigma Aldrich, supplied by Gold Biotechnology Inc, 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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New England Biolabs peptides
Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative <t>control</t> <t>RGD</t> (Con) or <t>RGDS</t> (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.
Peptides, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
FUJIFILM flt3 ligand
Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative <t>control</t> <t>RGD</t> (Con) or <t>RGDS</t> (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.
Flt3 Ligand, supplied by FUJIFILM, 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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92
R&D Systems nd recombinant human tgf beta 1 protein r d systems
Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative <t>control</t> <t>RGD</t> (Con) or <t>RGDS</t> (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.
Nd Recombinant Human Tgf Beta 1 Protein R D Systems, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cntf+chemicals%2C+peptides%2C+and+recombinant+proteins/Recombinant+Mouse+Nodal+Protein/pm32693087-256-60-66
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96
Jackson Immuno peptides
Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative <t>control</t> <t>RGD</t> (Con) or <t>RGDS</t> (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.
Peptides, supplied by Jackson Immuno, 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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Vector Laboratories peptides
Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative <t>control</t> <t>RGD</t> (Con) or <t>RGDS</t> (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.
Peptides, supplied by Vector Laboratories, 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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Image Search Results


Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative control RGD (Con) or RGDS (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.

Journal: Journal of sport and health science

Article Title: BMAL1/PGC1α4-FNDC5/irisin axis impacts distinct outcomes of time-of-day resistance exercise.

doi: 10.1016/j.jshs.2024.100968

Figure Lengend Snippet: Fig. 7. Irisin increased muscle hypertrophy via aV class of integrins and FAK-AKT-CREB signaling. Representative western blot analysis and quantification of (A) integrin-like signaling FAK-AKT-CREB phosphorylation and (B) Quantitative Polymerase Chain Reaction (qPCR) analysis in differentiated C2C12 myotubes pre-treated with negative control RGD (Con) or RGDS (10 uM) for 10 min and then treated with recombinant irisin (600 ng/mL) or His-tag (600 ng/mL). Repre- sentative Western blot analysis and quantification of (C) integrin-like signaling FAK-AKT-CREB phosphorylation and (D) qPCR analysis of IL6 in gastrocnemius muscle (GAS) from mice i.p. injected with His-tag or recombinant irisin (1mg/kg) and treated with negative control RGD (Con) or cRGDyK (1mg/kg) peptide every day for 2 weeks. (E) Mice were treated with integrin aV inhibitor cRGDyK (1 mg/kg) or negative control RGD (Con) for 48 h and their grip strength was assessed at late rest (LR) or late active (LA) phase. n = 6 per group. Percentage of (F) body weight change, (G) representative Hematoxylin and Eosin (H&E) staining, and (H) quantification of average fiber sizes of GAS muscles from mice i.p. injected with His-tag or recombinant irisin (1 mg/kg) in the combination of negative control RGD peptide (Con) or cRGDyK (1 mg/kg) every day for 2 weeks. n = 4 per group. Scale bar = 100 um. All data were shown as mean § SEM. Two-tailed unpaired Student’s t test was used for statistical comparison. *p < 0.05; ** p < 0.01. C2C12 = C2 myoblast cell line 12; GAPDH = Glyceraldehyde-3- phosphate Dehydrogenase; ns = not significant; RGDS = Arg-Gly-Asp-Ser.

Article Snippet: For quantitative real-time-polymerase chain reaction (qRT-PCR) and western blot analysis, differentiated C2C12 myotubes were pre-treated with 10 mM negative control Arginyl-glycyl-aspartic acid (RGD) (GL Biochem Chemicals, Shanghai, China) or RGDS (S8008; Selleck Chemicals, Houston, TX, USA) and administrated with recombinant irisin or His-tag at 600 ng/mL for indicated time.

Techniques: Western Blot, Phospho-proteomics, Real-time Polymerase Chain Reaction, Negative Control, Recombinant, Injection, Staining, Muscles, Two Tailed Test, Comparison