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TPPB has been demonstrated to activate PKC in this cell line, this effect was seen with TPPB doses in the order of 10–1,000 × g greater than those used for bryostatin-1 in the current studies. Therefore, when comparing bryostatin-1 and TPPB, a recognized APP modulator, bryostatin-1 was found to potently activate PKC-ε translocation in SH-SY5Y cells at 10−8, 10−9, and 10−10 (at 3 h).
| Cell Experiment | |
|---|---|
| Cell lines | SH-SY5Y neuroblastoma cells |
| Preparation method | Cells were grown to confluency in 10 % serum-supplemented medium. Dilutions of bryostatin-1 or TPPB were added to serum-free culture medium at various concentrations and treatments maintained for 3 h, except in time course experiments where several time points up to 24 h were taken. Pilot studies showed no change in SH-SY5Y appearance, attachment, or cell density for at least 24 h under these conditions. |
| Concentrations | 10 μM |
| Incubation time | 24 h |
| Animal Experiment | |
|---|---|
| Animal models | |
| Formulation | |
| Dosages | |
| Administration | |
| Molecular Weight | 501.54 |
| Formula | C27H30F3N3O3 |
| CAS Number | 497259-23-1 |
| Form | Solid |
| Solubility (25°C) | DMSO ≥ 100 mg/mL |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
| Related PKC Products |
|---|
| Enzastaurin
Enzastaurin inhibits PKCβ, PKCα, PKCγ and PKCε with IC50's of 0.006, 0.039, 0.083 and 0.110 µM, respectively. |
| Go 6983
Go 6983 is a fast acting, lipid soluble, broad spectrum protein kinase C inhibitor. |
| Staurosporine
Staurosporine (AM-2282) is a potent ATP-competitive kinase inhibitor with IC50 of 0.7, 7, 8.5, 6, 20 nM for PKC, PKA,PKG, p60v-src tyrosine protein kinase, CaM kinase II, respectively. |
| Zoledronic acid
Zoledronic Acid (Zoledronate) is a third-generation bisphosphonate (BP), with potent anti-resorptive activity. Zoledronic Acid inhibits the differentiation and apoptosis of osteoclasts. Zoledronic Acid also has anti-cancer effects. |
| Dequalinium Chloride
Dequalinium Chloride is a PKC inhibitor with IC50 of 7-18 μM, and also a selective blocker of apamin-sensitive K+ channels with IC50 of 1.1 μM. |
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