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Merck

900393

Sigma-Aldrich

Folate-PEG2000-COOH

average Mn 2,000

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About This Item

线性分子式:
C19H19N8O5(C2H4O)nC2H3O2
分類程式碼代碼:
51171641
NACRES:
NA.23

形狀

powder

品質等級

分子量

average Mn 2,000

轉變溫度

Tm 39-49 °C

儲存溫度

−20°C

應用

The folate end group may be used for target-specific cellular uptake of drug delivery vehicles and the carboxylate group can be used for further conjugation to make drug conjugates, polymeric nanoparticles, or folate targeting liposomes.

法律資訊

Product of JenKem Technology.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Da-Wen Dong et al.
Biomaterials, 34(20), 4849-4859 (2013-04-02)
A nanocarrier delivery system that can simultaneously deliver a chemotherapeutic drug and siRNA to the tumor is emerging as a promising treatment strategy for cancer treatment. In this study, a multifunctional PHD/PPF/siRNA complexes was developed by one-step assembly of prefunctionalized
Dipanjan Pan et al.
Chemical communications (Cambridge, England), (19)(19), 2400-2401 (2003-11-01)
Shell cross-linked nanoparticles (SCKs) constitute a unique class of materials with amphiphilic core-shell morphology; SCKs are characterised by their structural integrity and available functionality to attach receptor-recognising or receptor-specific ligands on the shell surface and, therefore, hold great potential in
Hyuk Sang Yoo et al.
Journal of controlled release : official journal of the Controlled Release Society, 100(2), 247-256 (2004-11-17)
For folate-receptor-targeted anti-cancer therapy, doxorubicin aggregates in a nano-scale size were produced employing doxorubicin-polyethylene glycol-folate (DOX-PEG-FOL) conjugate. Doxorubicin and folate were respectively conjugated to alpha- and omega-terminal end group of a PEG chain. The conjugates assisted to form doxorubicin nano-aggregates
Sun Hwa Kim et al.
Langmuir : the ACS journal of surfaces and colloids, 21(19), 8852-8857 (2005-09-07)
Poly(D,L-lactic-co-glycolic acid) (PLGA) nanoparticles with anionic surface charge were surface coated with cationic di-block copolymer, poly(L-lysine)-poly(ethylene glycol)-folate (PLL-PEG-FOL) conjugate, for enhancing their site-specific intracellular delivery against folate receptor overexpressing cancer cells. The PLGA nanoparticles coated with the conjugate were characterized

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