A cationic cell-penetrating peptide
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(Arg)9 is a cationic cell-penetrating peptide.1,2 It has been used to deliver various cargo to cells, including fluorescent proteins and plasmids. (Arg)9 (5 and 10 ?M) also protects primary rat cortical neurons from glutamate-induced excitotoxicity.3
1.Chang, M., Chou, J.-C., and Lee, H.-J.Cellular internalization of fluorescent proteins via arginine-rich intracellular delivery peptide in plant cellsPlant Cell Physiol.46(3)482-488(2005) 2.Lee, C.-Y., Li, J.-F., Liou, J.-S., et al.A gene delivery system for human cells mediated by both a cell-penetrating peptide and a piggyBac transposaseBiomaterials32(26)6264-6276(2011) 3.Meloni, B.P., Brookes, L.M., Clark, V.W., et al.Poly-arginine and arginine-rich peptides are neuroprotective in stroke modelsJ. Cereb. Blood Flow Metab.35(6)993-1004(2015)
Cell experiment: | (Arg)9 is prepared as 100× stocks (500 μM) in normal saline and assessed in a concentration range from 0.1 to 15 μM. (Arg)9 is added to culture 96-well plate 15 min prior to glutamic acid or kainic acid exposure. Neuronal viability is quantitatively using the MTS assay[1]. |
Animal experiment: | Rats: (Arg)9 (D-isoform) is prepared in 100× stocks (500?μM in water and assessed in a concentration range from 0.1 to 20?μM. Rats are fasted overnight and subjected to filament permanent middle cerebral artery occlusion (MCAO). Thirty minutes post-MCAO rats are intravenously treated with (Arg)9 (1?μmol/kg in 600?μL over 5 minutes) or vehicle (normal saline for injection; 600?μL over 5 minutes). Treatments are randomized and all procedures are performed masked to treatment. Twenty-four hours post-MCAO infarct area assessment is performed[2]. |
参考文献: [1]. Meloni BP, et al. The neuroprotective efficacy of cell-penetrating peptides TAT, penetratin, Arg-9, and Pep-1 in glutamic acid, kainic acid, and in vitro ischemia injury models using primary cortical neuronal cultures. Cell Mol Neurobiol. 2014 Mar;34(2):173-81. |
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