676494

VEGF Inhibitor, Je-11 - Calbiochem

• 别名: VEGF Inhibitor, Je-11 - Calbiochem, (RTELNVGIDFNWEYPAS)₂K-NH₂, VEGFR Tyrosine Kinase Inhibitor XI, VEGFR2 Kinase Inhibitor XII
• 经验公式（希尔记法）: C₁₈₈H₂₇₃N₄₉O₅₇
• 分子量: 4131.47
• 分類程式碼代碼: 12352200

属性

• 化驗: ≥90% (HPLC)
• 品質等級: 100
• 形狀: lyophilized solid
• 製造商／商標名: Calbiochem^®
• 儲存條件: OK to freeze; desiccated (hygroscopic)
• 顏色: white
• 溶解度: DMSO: 5 mg/mL
• 運輸包裝: ambient
• 儲存溫度: 2-8°C

说明

一般說明

This product has been discontinued.

A dimerized peptide derived from the third Ig-like domain of the human vascular endothelial growth factor receptor-2 (VEGFR-2 or KDR/Flk-1) comprising residues 247 - 261. Acts as an inhibitor of VEGF-stimulated autophosphorylation of VEGFR-2 and inhibits the proliferation and migration of cultured microvascular endothelial cells. Binds to VEGF and blocks its interaction with VEGFR-2 (IC₅₀ = 500 nM on extracellular VEGFR-2 fragments; IC₅₀ = 30 µM on HUVEC).

A dimerized peptide derived from the third Ig-like domain of the human vascular endothelial growth factor receptor-2 (VEGFR-2 or KDR/FLK-1) comprising residues 247-261. Acts as an inhibitor of VEGF-stimulated autophosphorylation of VEGFR-2 (IC₅₀ = 500 nM on extracellular VEGFR-2 fragments; IC₅₀ = 30 µM on HUVEC).

生化／生理作用

Cell permeable: no

Primary Target
Binds to VEGF and blocks its interaction with VEGFR-2

Product does not compete with ATP.

Reversible: no

Target IC₅₀: 500 nM on extracellular VEGFR-2 fragments; 30 µM on HUVEC

包裝

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

序列

(H-Arg-Thr-Glu-Leu-Asn-Val-Gly-Ile-Asp-Phe-Asn-Trp-Glu-Tyr-Pro-Ala-Ser)₂-Lys-NH₂

外觀

Supplied as a trifluoroacetate salt.

重構

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

其他說明

Piossek, C., et al. 1999. J. Biol. Chem.274, 5612.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

安全信息

• 儲存類別代碼: 10-13 - German Storage Class 10 to 13