a23187 (Alomone Labs)


Structured Review

A23187, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 92/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/a23187/product/Alomone Labs
Average 92 stars, based on 11 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells"
Article Title: A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells
Journal: International Journal of Nanomedicine
doi: 10.2147/IJN.S168149

Figure Legend Snippet: Membrane-permeable CPP-MT and CPP-MT-AuNP inhibit acrosomal exocytosis in sperm. Notes: Human sperm were incubated for 1 hour at 37°C in HTF medium with increasing concentrations of recombinant CPP-MT unconjugated ( A ) or conjugated to AuNPs ( B ). Afterward, the cells were incubated for 15 minutes without stimulus (control) or with 10 µM A23187. After incubation, the samples were fixed and the acrosomal exocytosis index was evaluated using PSL-FITC and calculated as detailed in section “Materials and methods”. The data represent mean values ± SEM and were calculated from three independent experiments. Two-way ANOVA shows statistically significant difference (*** P
Techniques Used: Conditioned Place Preference, Incubation, Recombinant
2) Product Images from "MARCKS Protein Is Phosphorylated and Regulates Calcium Mobilization during Human Acrosomal Exocytosis"
Article Title: MARCKS Protein Is Phosphorylated and Regulates Calcium Mobilization during Human Acrosomal Exocytosis
Journal: PLoS ONE
doi: 10.1371/journal.pone.0064551

Figure Legend Snippet: Assessing MARCKS function on acrosomal exocytosis in non-permeabilized sperm. ( A ) Capacitated and non-permeabilized sperm were treated for 30 minutes at 37°C with increasing concentrations of a permeable tetramethylrhodamine-labeled MARCKS ED peptide (ED-TMR). Acrosomal exocytosis was then initiated by adding 10 µM calcium ionophore A23187 (circles), 200 nM PMA (squares) or 15 µM progesterone (triangles), and the incubation continued for 15 minutes. The percentage of reacted sperm was normalized as described in Materials and Methods . The data represent the means±SEM of at least three independent experiments. The asterisks indicate significant differences from similar conditions without ED-TMR (*, p
Techniques Used: Labeling, Incubation
3) Product Images from "MARCKS Protein Is Phosphorylated and Regulates Calcium Mobilization during Human Acrosomal Exocytosis"
Article Title: MARCKS Protein Is Phosphorylated and Regulates Calcium Mobilization during Human Acrosomal Exocytosis
Journal: PLoS ONE
doi: 10.1371/journal.pone.0064551

Figure Legend Snippet: Assessing MARCKS function on acrosomal exocytosis in non-permeabilized sperm. ( A ) Capacitated and non-permeabilized sperm were treated for 30 minutes at 37°C with increasing concentrations of a permeable tetramethylrhodamine-labeled MARCKS ED peptide (ED-TMR). Acrosomal exocytosis was then initiated by adding 10 µM calcium ionophore A23187 (circles), 200 nM PMA (squares) or 15 µM progesterone (triangles), and the incubation continued for 15 minutes. The percentage of reacted sperm was normalized as described in Materials and Methods . The data represent the means±SEM of at least three independent experiments. The asterisks indicate significant differences from similar conditions without ED-TMR (*, p
Techniques Used: Labeling, Incubation
4) Product Images from "Novel phenotype in beagle dogs characterized by skin response to compound 48/80 focusing on skin mast cell degranulation"
Article Title: Novel phenotype in beagle dogs characterized by skin response to compound 48/80 focusing on skin mast cell degranulation
Journal: Experimental Animals
doi: 10.1538/expanim.15-0004

Figure Legend Snippet: Illustration of main pathways to skin response via mast cells based on results shown in Fig. 4 . Nonresponder dogs showed skin responses to HCO-60, histamine dihydrochloride, concanavalin A, and A23187 comparable to those of wild-type dogs but no response to compound 48/80; the dysfunctional route in NR dogs would be downstream of the GPCR.
Techniques Used:

Figure Legend Snippet: Vascular permeability to various compounds. Compound 48/80 (A), HCO-60 (B), histamine dihydrochloride (C), concanavalin A (D), and A23187 (E) at 0.01–100 mg/ml ID injected at 0.05 ml/site into the shaved thorax of anesthetized wild-type (WT) and nonresponder (NR) dogs; Evans blue (1 mg/kg) dissolved in saline IV injected just prior to ID injections; and 10 min later, ID injection sites collected for determination of pigment leakage. The significance of the differences between WT and NR groups was determined by Student’s t -test. ** P
Techniques Used: Permeability, Injection
5) Product Images from "A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells"
Article Title: A TEM-traceable physiologically functional gold nanoprobe that permeates non-endocytic cells
Journal: International Journal of Nanomedicine
doi: 10.2147/IJN.S168149

Figure Legend Snippet: Membrane-permeable CPP-MT and CPP-MT-AuNP inhibit acrosomal exocytosis in sperm. Notes: Human sperm were incubated for 1 hour at 37°C in HTF medium with increasing concentrations of recombinant CPP-MT unconjugated ( A ) or conjugated to AuNPs ( B ). Afterward, the cells were incubated for 15 minutes without stimulus (control) or with 10 µM A23187. After incubation, the samples were fixed and the acrosomal exocytosis index was evaluated using PSL-FITC and calculated as detailed in section “Materials and methods”. The data represent mean values ± SEM and were calculated from three independent experiments. Two-way ANOVA shows statistically significant difference (*** P
Techniques Used: Incubation, Recombinant
6) Product Images from "Novel phenotype in beagle dogs characterized by skin response to compound 48/80 focusing on skin mast cell degranulation"
Article Title: Novel phenotype in beagle dogs characterized by skin response to compound 48/80 focusing on skin mast cell degranulation
Journal: Experimental Animals
doi: 10.1538/expanim.15-0004

Figure Legend Snippet: Illustration of main pathways to skin response via mast cells based on results shown in Fig. 4 . Nonresponder dogs showed skin responses to HCO-60, histamine dihydrochloride, concanavalin A, and A23187 comparable to those of wild-type dogs but no response to compound 48/80; the dysfunctional route in NR dogs would be downstream of the GPCR.
Techniques Used:

Figure Legend Snippet: Vascular permeability to various compounds. Compound 48/80 (A), HCO-60 (B), histamine dihydrochloride (C), concanavalin A (D), and A23187 (E) at 0.01–100 mg/ml ID injected at 0.05 ml/site into the shaved thorax of anesthetized wild-type (WT) and nonresponder (NR) dogs; Evans blue (1 mg/kg) dissolved in saline IV injected just prior to ID injections; and 10 min later, ID injection sites collected for determination of pigment leakage. The significance of the differences between WT and NR groups was determined by Student’s t -test. ** P
Techniques Used: Permeability, Injection