NLS-StAx-h

NLS-StAx-h;

NLS-StAx-h 是选择性的 Wnt 信号传导的固定肽抑制剂,IC50 为 1.4 μM。NLS-StAx-h 有效抑制 β-catenin-转录因子的相互作用。NLS-StAx-h 抑制结直肠癌细胞的增殖和迁移。

NLS-StAx-hamp;;

NLS-StAx-h Chemical Structure

规格 是否有货
100 μg 询价

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生物活性

NLS-StAx-h is a selective, stapled peptide inhibitor of Wnt signaling with an IC50 of 1.4 μM. NLS-StAx-h efficiently inhibits β-catenin-transcription factor interactions. NLS-StAx-h inhibits proliferation and migration of colorectal cancer cells[1].

IC50 Target[1]

Wnt

1.4 mu;M (IC50)

体外研究
(In Vitro)

NLS-StAx-h (10 μM, 72 hr) reduces the viability of both SW-480 and DLD-1 by more than 80%. NLS-StAx-h results in gene expression changes[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

3445.26

Formula

C53H100N19O10V2W

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Laura Dietrich, et al. Cell Permeable Stapled Peptide Inhibitor of Wnt Signaling That Targets β-Catenin Protein-Protein Interactions