G3892
Gly-Arg-Gly-Asp
≥97% (HPLC)
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About This Item
Análisis
≥97% (HPLC)
temp. de almacenamiento
−20°C
cadena SMILES
NCC(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC(O)=O)C(O)=O
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Otras notas
Tetrapeptide overlapping the cell-attachment domain of fibronectin (the cell-attachment promoting activity has been localized to the tetrapeptide Arg-Gly-Asp-Ser).
Código de clase de almacenamiento
13 - Non Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
Certificados de análisis (COA)
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Peptides, 24(8), 1109-1115 (2003-11-13)
Continuing our research on Mycobacteria kansasii phagocytosis inhibition, we have examined in that context three series of peptides derived from the RGDVY and GRGD sequences. It was found that the levels of the inhibitory activity depend on the amino acid
Biomaterials, 23(24), 4803-4809 (2002-10-04)
To improve ECs adhesion and growth on chitosan, cell adhesive peptide Gly-Arg-Gly-Asp (GRGD) was photochemically grafted to its surface. Grafting 0.025 M of GRGD-SANPAH (N-Succinimidyl-6-[4'-azido-2'-nitrophenylamino]-hexanoate) solutions to chitosan and tripolyphosphate anhydrous crosslinked chitosan (chitosan-TPP) surfaces was performed by surface adsorption
Journal of biomedical materials research. Part A, 91(3), 753-761 (2008-12-04)
Accelerated thrombolysis by pressure-driven permeation has been demonstrated in in vitro and in vivo animal models by using plasminogen activators (PAs) encapsulated liposomes or PEG microparticles. Recent reports have also described acceleration of thrombolysis using tissue type PA (t-PA) encapsulated
Artificial organs, 25(8), 617-621 (2001-09-05)
To improve endothelial cell adhesion and growth on the surface of polyethylene glycol modified polyurethane (PU-PEG), cell adhesive peptide Gly-Arg-Gly-Asp (GRGD) was photochemically grafted to the surface. The surface grafted GRGD-N-Succinimidyl-6-[4'-azido-2'-nitrophenylamino]hexanoate (SANPAH) on a PU-PEG surface was performed by adsorption
Cancer research, 56(13), 3103-3111 (1996-07-01)
The molecules that mediate metastatic cell homing to specific organ sites remain largely unidentified. As a target organ for metastasis, the liver is a unique environment characterized by fenestrated sinusoidal endothelium, lack of a complete basement membrane, and production of
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