aspergillus niger s Search Results


aspergillus niger s-58  (METTLER TOLEDO)
90
METTLER TOLEDO aspergillus niger s-58
Aspergillus Niger S 58, supplied by METTLER TOLEDO, 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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Average 90 stars, based on 1 article reviews
aspergillus niger s-58 - by Bioz Stars, 2026-05
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α7nachr  (Databank Inc)
86
Databank Inc α7nachr
Effects of Liraglutide on LPS-induced PG elevations in the presence and absence of non-selective nAChR or <t>α7nAChR</t> antagonists. Shown are the effects of liraglutide (10 nM) on 1 µg/ml LPS -induced Prostaglandin E2 ( A ), 6-keto prostaglandin F1α ( B ), Thromboxane A2 ( C ) levels with or without mecamylamine (MEC, 50 μΜ) or methyllycaconitine (MLA, 1 μΜ). Data are shown as mean ± S.E.M. (*, p < 0.05 vs control; †, p < 0.05 vs LPS group; ‡, p < 0.05, vs LPS + VAR, n = 6). LPS: Lipopolysaccharide, MEC: mecamylamine, MLA: methyllycaconitine
α7nachr, supplied by Databank Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/α7nachr/product/Databank Inc
Average 86 stars, based on 1 article reviews
α7nachr - by Bioz Stars, 2026-05
86/100 stars
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Effects of Liraglutide on LPS-induced PG elevations in the presence and absence of non-selective nAChR or α7nAChR antagonists. Shown are the effects of liraglutide (10 nM) on 1 µg/ml LPS -induced Prostaglandin E2 ( A ), 6-keto prostaglandin F1α ( B ), Thromboxane A2 ( C ) levels with or without mecamylamine (MEC, 50 μΜ) or methyllycaconitine (MLA, 1 μΜ). Data are shown as mean ± S.E.M. (*, p < 0.05 vs control; †, p < 0.05 vs LPS group; ‡, p < 0.05, vs LPS + VAR, n = 6). LPS: Lipopolysaccharide, MEC: mecamylamine, MLA: methyllycaconitine

Journal: Naunyn-Schmiedeberg's Archives of Pharmacology

Article Title: Liraglutide modulates cyclooxygenase and α7 acetylcholine receptors: in vitro and in silico insights into its anti-inflammatory role in LPS-induced inflammation in RAW 264.7 macrophages

doi: 10.1007/s00210-025-04225-5

Figure Lengend Snippet: Effects of Liraglutide on LPS-induced PG elevations in the presence and absence of non-selective nAChR or α7nAChR antagonists. Shown are the effects of liraglutide (10 nM) on 1 µg/ml LPS -induced Prostaglandin E2 ( A ), 6-keto prostaglandin F1α ( B ), Thromboxane A2 ( C ) levels with or without mecamylamine (MEC, 50 μΜ) or methyllycaconitine (MLA, 1 μΜ). Data are shown as mean ± S.E.M. (*, p < 0.05 vs control; †, p < 0.05 vs LPS group; ‡, p < 0.05, vs LPS + VAR, n = 6). LPS: Lipopolysaccharide, MEC: mecamylamine, MLA: methyllycaconitine

Article Snippet: Initially, crystal structures of α7nAChR, COX-2, PGIS, Liraglutide, and GLP-1 were downloaded from Protein DataBank (PDB IDs: 7EKP, 3LN1, 3B6H, 4 APD, and 3IOL, respectively).

Techniques: Control

Predicted interactions of liraglutide (PDB: 4 APD) with ( A ) α7nAChR (PDB: 7EKP), B COX-2 (PDB: 3LN1), and C Prostacyclin Synthase (PDB: 3B6H) modeled with HADDOCK 2.4. protein–protein docking server

Journal: Naunyn-Schmiedeberg's Archives of Pharmacology

Article Title: Liraglutide modulates cyclooxygenase and α7 acetylcholine receptors: in vitro and in silico insights into its anti-inflammatory role in LPS-induced inflammation in RAW 264.7 macrophages

doi: 10.1007/s00210-025-04225-5

Figure Lengend Snippet: Predicted interactions of liraglutide (PDB: 4 APD) with ( A ) α7nAChR (PDB: 7EKP), B COX-2 (PDB: 3LN1), and C Prostacyclin Synthase (PDB: 3B6H) modeled with HADDOCK 2.4. protein–protein docking server

Article Snippet: Initially, crystal structures of α7nAChR, COX-2, PGIS, Liraglutide, and GLP-1 were downloaded from Protein DataBank (PDB IDs: 7EKP, 3LN1, 3B6H, 4 APD, and 3IOL, respectively).

Techniques:

Predicted interactions of GLP-1 (PDB: 3IOL) with ( A ) Alpha 7 Nicotinic Acetylcholine Receptor (PDB: 7EKP), B COX-2 (PDB: 3LN1), and C Prostacyclin Synthase (PDB: 3B6H) modeled with HADDOCK 2.4. protein–protein docking server

Journal: Naunyn-Schmiedeberg's Archives of Pharmacology

Article Title: Liraglutide modulates cyclooxygenase and α7 acetylcholine receptors: in vitro and in silico insights into its anti-inflammatory role in LPS-induced inflammation in RAW 264.7 macrophages

doi: 10.1007/s00210-025-04225-5

Figure Lengend Snippet: Predicted interactions of GLP-1 (PDB: 3IOL) with ( A ) Alpha 7 Nicotinic Acetylcholine Receptor (PDB: 7EKP), B COX-2 (PDB: 3LN1), and C Prostacyclin Synthase (PDB: 3B6H) modeled with HADDOCK 2.4. protein–protein docking server

Article Snippet: Initially, crystal structures of α7nAChR, COX-2, PGIS, Liraglutide, and GLP-1 were downloaded from Protein DataBank (PDB IDs: 7EKP, 3LN1, 3B6H, 4 APD, and 3IOL, respectively).

Techniques: