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Eppendorf AG g s6
G S6, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 96/100, based on 114 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Article Title: Zn 3 (PO 4 ) 2 shell effects on Zn uptake and cellular distribution of root applied ZnO NPs
Article Snippet: Aliquots were taken from the tubes after 1 and 6 weeks and centrifuged for 30 min at 16,392 g S6 (Eppendorf® 5415R, rotor: F-45-24-11).



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The hepatic content of phosphorylated proteins from insulin transduction pathway, i.e., insulin receptor substrate 1 (pIRS1(Ser636/Ser639), ( A )), phosphate and tensin homolog (pPTEN(Ser380), ( B )), protein kinase B (pAkt(Ser473), ( C )), glycogen synthase kinase 3α/β (pGSK3α/β(Ser21/Ser9), ( D )), Bcl-2-associated agonist of cell death (pBAD(Ser136), ( E )), mechanistic target of rapamycin (pmTOR(Ser2448), ( F )), P70 ribosomal protein S6 kinase (pP70 S6 kinase(Thr389), ( G )) and S6 ribosomal protein (pS6RP(Ser235/Ser236), ( H )) in rats subjected to a standard diet (Control) or a high-fat diet (HFD) after α-lipoic acid (α-LA) administration for eight weeks. Magnetic bead-related immunoassay-measured phosphorylated proteins’ fluorescent intensity (FI). The results are presented as mean ± standard deviation (SD) and established on ten independent determinations in each experimental group. * p < 0.05—significant differences vs. Control group. # p < 0.05—significant differences vs. HFD group.

Journal: Nutrients

Article Title: Hepatic-Metabolic Activity of α-Lipoic Acid—Its Influence on Sphingolipid Metabolism and PI3K/Akt/mTOR Pathway in a Rat Model of Metabolic Dysfunction-Associated Steatotic Liver Disease

doi: 10.3390/nu16101501

Figure Lengend Snippet: The hepatic content of phosphorylated proteins from insulin transduction pathway, i.e., insulin receptor substrate 1 (pIRS1(Ser636/Ser639), ( A )), phosphate and tensin homolog (pPTEN(Ser380), ( B )), protein kinase B (pAkt(Ser473), ( C )), glycogen synthase kinase 3α/β (pGSK3α/β(Ser21/Ser9), ( D )), Bcl-2-associated agonist of cell death (pBAD(Ser136), ( E )), mechanistic target of rapamycin (pmTOR(Ser2448), ( F )), P70 ribosomal protein S6 kinase (pP70 S6 kinase(Thr389), ( G )) and S6 ribosomal protein (pS6RP(Ser235/Ser236), ( H )) in rats subjected to a standard diet (Control) or a high-fat diet (HFD) after α-lipoic acid (α-LA) administration for eight weeks. Magnetic bead-related immunoassay-measured phosphorylated proteins’ fluorescent intensity (FI). The results are presented as mean ± standard deviation (SD) and established on ten independent determinations in each experimental group. * p < 0.05—significant differences vs. Control group. # p < 0.05—significant differences vs. HFD group.

Article Snippet: The hepatic level of phosphorylated proteins from the insulin signaling pathway, i.e., insulin receptor substrate 1 (pIRS1(Ser636/Ser639)), phosphate and tensin homolog (pPTEN(Ser380)), protein kinase B (pAkt(Ser473)), glycogen synthase kinase 3α/β (pGSK3α/β(Ser21/Ser9)), Bcl-2-associated agonist of cell death (pBAD(Ser136)), mechanistic target of rapamycin (pmTOR(Ser2448)), P70 ribosomal protein S6 kinase (pP70 S6 kinase(Thr389)) and S6 ribosomal protein (pS6RP(Ser235/Ser236)) was assessed using a Bio-Plex Pro Cell Signaling Assays (Bio-Rad, Hercules, CA, USA).

Techniques: Transduction, Control, Standard Deviation

The hepatic content of phosphorylated proteins from insulin transduction pathway, i.e., insulin receptor substrate 1 (pIRS1(Ser636/Ser639), ( A )), phosphate and tensin homolog (pPTEN(Ser380), ( B )), protein kinase B (pAkt(Ser473), ( C )), glycogen synthase kinase 3α/β (pGSK3α/β(Ser21/Ser9), ( D )), Bcl-2-associated agonist of cell death (pBAD(Ser136), ( E )), mechanistic target of rapamycin (pmTOR(Ser2448), ( F )), P70 ribosomal protein S6 kinase (pP70 S6 kinase(Thr389), ( G )) and S6 ribosomal protein (pS6RP(Ser235/Ser236), ( H )) in rats subjected to a standard diet (Control) or a high-fat diet (HFD) after α-lipoic acid (α-LA) administration for eight weeks. Magnetic bead-related immunoassay-measured phosphorylated proteins’ fluorescent intensity (FI). The results are presented as mean ± standard deviation (SD) and established on ten independent determinations in each experimental group. * p < 0.05—significant differences vs. Control group. # p < 0.05—significant differences vs. HFD group.

Journal: Nutrients

Article Title: Hepatic-Metabolic Activity of α-Lipoic Acid—Its Influence on Sphingolipid Metabolism and PI3K/Akt/mTOR Pathway in a Rat Model of Metabolic Dysfunction-Associated Steatotic Liver Disease

doi: 10.3390/nu16101501

Figure Lengend Snippet: The hepatic content of phosphorylated proteins from insulin transduction pathway, i.e., insulin receptor substrate 1 (pIRS1(Ser636/Ser639), ( A )), phosphate and tensin homolog (pPTEN(Ser380), ( B )), protein kinase B (pAkt(Ser473), ( C )), glycogen synthase kinase 3α/β (pGSK3α/β(Ser21/Ser9), ( D )), Bcl-2-associated agonist of cell death (pBAD(Ser136), ( E )), mechanistic target of rapamycin (pmTOR(Ser2448), ( F )), P70 ribosomal protein S6 kinase (pP70 S6 kinase(Thr389), ( G )) and S6 ribosomal protein (pS6RP(Ser235/Ser236), ( H )) in rats subjected to a standard diet (Control) or a high-fat diet (HFD) after α-lipoic acid (α-LA) administration for eight weeks. Magnetic bead-related immunoassay-measured phosphorylated proteins’ fluorescent intensity (FI). The results are presented as mean ± standard deviation (SD) and established on ten independent determinations in each experimental group. * p < 0.05—significant differences vs. Control group. # p < 0.05—significant differences vs. HFD group.

Article Snippet: The hepatic level of phosphorylated proteins from the insulin signaling pathway, i.e., insulin receptor substrate 1 (pIRS1(Ser636/Ser639)), phosphate and tensin homolog (pPTEN(Ser380)), protein kinase B (pAkt(Ser473)), glycogen synthase kinase 3α/β (pGSK3α/β(Ser21/Ser9)), Bcl-2-associated agonist of cell death (pBAD(Ser136)), mechanistic target of rapamycin (pmTOR(Ser2448)), P70 ribosomal protein S6 kinase (pP70 S6 kinase(Thr389)) and S6 ribosomal protein (pS6RP(Ser235/Ser236)) was assessed using a Bio-Plex Pro Cell Signaling Assays (Bio-Rad, Hercules, CA, USA).

Techniques: Transduction, Control, Standard Deviation