D9885
DEAE-Dextran hydrochloride
powder
Synonym(s):
Diethylaminoethyl-dextran hydrochloride
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About This Item
Product Name
DEAE-Dextran hydrochloride, powder
biological source
bacterial (Leuconostoc mesenteroides)
form
powder
extent of labeling
~3.2% nitrogen
useful pH range
4.0 - 6.0
solubility
H2O: soluble 100 mg/mL, clear, colorless to faintly yellow
storage temp.
room temp
Quality Level
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Application
DEAE-Dextran 500, a polycationic stabilizing molecule and transfection reagent, is used in the development of sustained release protein delivery and nucleic acid transfection systems. DEAE-Dextran 500 may be used for cell immobilization in biosensors.
Other Notes
To gain a comprehensive understanding of our extensive range of Dextrans for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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DEAE-dextran transfection of mammalian cultured cells.
E T Schenborn et al.
Methods in molecular biology (Clifton, N.J.), 130, 147-153 (1999-12-10)
Transfection using DEAE-dextran.
Selden RF.
Current Protocols in Immunology, 10, 10-10 (2001)
Anita Bogdanov et al.
Antimicrobial agents and chemotherapy, 58(1), 405-413 (2013-11-06)
Chlamydiae are obligate intracellular bacteria that propagate in the inclusion, a specific niche inside the host cell. The standard method for counting chlamydiae is immunofluorescent staining and manual counting of chlamydial inclusions. High- or medium-throughput estimation of the reduction in
Nattamon Niyomdecha et al.
Heliyon, 6(6), e04050-e04050 (2020-06-13)
Niclosamide has been known to inhibit a number of pH-dependent viruses via the neutralization of endosomal acidic pH. It has also been shown to disrupt the mTORC1 signaling pathway. The replication of many viruses requires mTORC1 activation. Here, we investigated
Shingo Kikuchi et al.
International journal of pharmaceutics, 386(1-2), 149-155 (2009-11-20)
A multivariate statistical technique was applied to designing a tablet for the sustained release over 24h of diltiazem hydrochloride, a model highly water-soluble drug. Tablets of a hydrophilic matrix composed of dextran derivatives and hypromellose were prepared. The formulations were
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