TAT-DEF-Elk-1;(Synonyms: TDE)
TAT-DEF-Elk-1 (TDE) 是 Elk-1 的一种可穿透细胞的肽抑制剂,通过模仿和特异性干扰 Elk-1 的 DEF 结构域来实现抑制。TAT-DEF-Elk-1 阻止 Elk-1 磷酸化并防止 Elk-1 核易位,且不会干扰 ERK 或 MSK1 活化。TAT-DEF-Elk-1 是分析神经元可塑性发展过程中 Elk-1 在此过程中的作用的有用工具。
TAT-DEF-Elk-1 Chemical Structure
CAS No. : 1220751-16-5
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生物活性 |
TAT-DEF-Elk-1 (TDE) is a cell-penetrating peptide inhibitor of Elk-1, mimics and specifically interferes with the DEF domain of Elk-1. TAT-DEF-Elk-1 blocks Elk-1 phosphorylation and prevents Elk-1 nuclear translocation without interfering with ERK nor MSK1 activation. TAT-DEF-Elk-1 is a useful tool to analyze the role of Elk-1 in this process during the development of neuronal plasticity[1]. |
IC50 Target |
IC50: Elk-1[1] |
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体外研究 (In Vitro) |
Elk-1 phosphorylation on Ser383/389 has a dual function and triggers both Elk-1 nuclear translocation and SRE-dependent gene expression[1].TAT-DEF-Elk-1 (5-10 μM; 1 hour) specifically inhibits glutamate-induced elk-1 activation and does not interfer with ERK, MSK-1, or CREB phosphorylation[1].TAT-DEF-Elk-1 (5 μM; 2 hour) treatment shows a significant inhibition of c-Fos, Zif268 and JunB, but has no effects on c-Jun expression[1]. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot Analysis[1]
RT-PCR[1]
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体内研究 (In Vivo) |
TAT-DEF-Elk-1 (intraperitoneal injection; 1mg/kg; daily; 14 days) reflects antidepressant efficacy in mice, it decreases immobility similar to the reference antidepressants fluoxetine and desipramine (DMI)[2]. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
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分子量 |
3561.07 |
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Formula |
C155H259N57O40 |
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CAS 号 |
1220751-16-5 |
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Sequence Shortening |
GRKKRRQRRRPPSPAKLSFQFPSSGSAQVHI |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
Please store the product under the recommended conditions in the Certificate of Analysis. |
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参考文献 |
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