Tat-NR2B9c TFA (Synonyms: Tat-NR2Bct TFA; NA-1 TFA) |
| Katalog-Nr.GC34828 |
Tat-NR2B9c TFA (Tat-NR2Bct TFA) ist ein Inhibitor der postsynaptischen Dichte 95 (PSD-95) mit EC50-Werten von 6,7 nM und 670 nM fÜr PSD-95d2 (PSD-95 PDZ-DomÄne 2) bzw. PSD-95d1 .
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1834571-04-8
Sample solution is provided at 25 µL, 10mM.
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Tat-NR2B9c (TFA) is a 20-aa peptide, which acts as a postsynaptic density-95 (PSD-95) inhibitor, with an EC50 of 6.7 nM for PSD-95d2 (PSD-95 PDZ domain 2), and 670 nM for PSD-95d1[1]. Tat-NR2B9c also reduces NMDA-induced p38 activation, and possesses neuroprotective efficacy[2]. EC50: 6.7 nM (PSD-95d2), 670 nM (PSD-95d1)[1]p38[2]
[1]. Cui H, et al. PDZ protein interactions underlying NMDA receptor-mediated excitotoxicity and neuroprotection by PSD-95 inhibitors. J Neurosci. 2007 Sep 12;27(37):9901-15. [2]. Fan J, et al. P38 MAPK is involved in enhanced NMDA receptor-dependent excitotoxicity in YAC transgenic mouse model of Huntington disease. Neurobiol Dis. 2012 Mar;45(3):999-1009.
Average Rating: 5 (Based on Reviews and 2 reference(s) in Google Scholar.)
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