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Pep2m, myristoylated TFA 
Pep2m, myristoylated TFA
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英文名稱 : Pep2m, myristoylated TFA
貨號 : EY-01Y12178
含量 : >99.00%
規(guī)格 : 5 mg
品牌 : 上海一研
價格 :
0.00
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產(chǎn)品屬性:


產(chǎn)品名稱

Pep2m, myristoylated TFA

規(guī)格

5 mg

貨號

EY-01Y12178

Cas No.: N/A

別名: N/A

化學(xué)名: N/A

分子式: C65H119F3N18O16S
GC61585.png
分子量: 1497.83

溶解度: N/A

儲存條件: -20°C, away from moisture
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.

Shipping ConditionEvaluation sample solution : ship with blue ice

All other available size: ship with RT , or blue ice upon request

產(chǎn)品描述:


Pep2m, myristoylated TFA (Myr-Pep2m TFA) is a cell-permeable peptide. Pep2m, myristoylated TFA can disrupt the protein kinase ζ (PKMζ) downstream targets, N-ethylmaleimide-sensitive factor/glutamate receptor subunit 2 (NSF/GluR2) interactions. PKMζ is an autonomously active isozyme of protein kinase C (PKC)[1][2].Pep2m, myristoylated TFA (10 μM) blocks PKMζ-mediated AMPA receptor (AMPAR) potentiation[1].Pep2m, myristoylated TFA does not block the increase of PKMζ in the hippocampal slices during long-term potentiation (LTP) maintenance, indicating that blocking NSF/GluR2 interactions do not prevent the induction of PKMζ synthesis[1].Pep2m, myristoylated TFA blocks NSF/GluR2-mediated AMPAR trafficking, and reverses persistent potentiation at both the strongly stimulates synapses and the weakly stimulats synapses that underwent synaptic tagging and capture[1].Pep2m, myristoylated TFA (10 μg) results in an increase in paw withdrawal thresholds (PWTs) on nociceptive responses in the formalin test[2].Animal Model:Female and male Long-Evans hooded rats (8 weeks)[2][1]. Yudong Yao, et al. PKMζ Maintains Late Long-Term Potentiation by N-Ethylmaleimide-Sensitive Factor/GluR2-Dependent Trafficking of Postsynaptic AMPA Receptors. J Neurosci. 2008 Jul 30; 28(31): 7820-7827.

[2]. Nicole C George, et al. Sex differences in the contributions of spinal atypical PKCs and downstream targets to the maintenance of nociceptive sensitization. Mol Pain. 2019; 15: 1744806919840582.
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