Chemical Structure : LCKLSL
CAS No.: 533902-29-3
货号: PC-24942Not For Human Use, Lab Use Only.
LCKLSL (Leu-Cys-Lys-Leu-Ser-Leu) is a potent, specific hexapeptide competitive inhibitor of Annexin A2 (AnxA2), inhibits tissue plasminogen activator (tPA)-binding capacity with IC50 of 11 uM.
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5 mg | ¥1880 | In stock | |
10 mg | ¥2980 | In stock | |
25 mg | ¥4980 | In stock | |
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LCKLSL (Leu-Cys-Lys-Leu-Ser-Leu) is a potent, specific hexapeptide competitive inhibitor of Annexin A2 (AnxA2), inhibits tissue plasminogen activator (tPA)-binding capacity with IC50 of 11 uM.
LCKLSL targets the N-terminal tPA-binding site of AnxA2, binds efficiently to cell-surface AnxA2 compared with binding of the control peptide LGKLSL.
LCKLSL inhibits the generation of plasmin and suppresses the VEGF-induced activity of tPA under hypoxic conditions.
LCKLSL prevents hypoxia-induced angiogenic events in in vivo models of angiogenesis.
分子量 | 675.89 | |
分子式 | C30H57N7O8S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
AA sequence: Leu-Cys-Lys-Leu-Ser-Leu |
1. Hajjar KA, et al. J Biol Chem. 1998 Apr 17;273(16):9987-93.
2. Valapala M, et al. J Cell Sci. 2011 May 1;124(Pt 9):1453-64.
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