form
liquid
InChI
1S/C25H44O/c1-21(2)11-7-12-22(3)13-8-14-23(4)15-9-16-24(5)17-10-18-25(6)19-20-26/h11,13,15,17,25-26H,7-10,12,14,16,18-20H2,1-6H3/b22-13+,23-15+,24-17-/t25-/m0/s1
InChI key
KLGBTYNAYAZPFD-YGRYZZMUSA-N
SMILES string
CC(C)=CCC/C(C)=C/CC/C(C)=C/CC/C(C)=C\CC[C@@H](CCO)C
assay
>99% (TLC)
packaging
pkg of 1 × 1 mg (900200O-1mg), pkg of 1 × 2 mg (900200O-2mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand
lipid type
neutral lipids
neutral glycerides
shipped in
dry ice
storage temp.
−20°C
General description
Dolichol is composed of repeated units of isoprenoids and forms a long chain unsaturated molecule. It is known to be widely present in all eukaryotic cells. Dolichol is predominantly synthesised in endoplasmic reticulum and localized to the phospholipid bilayer.
Biochem/physiol Actions
Dolichol influences the process of protein transfer in the endoplasmic reticulum through protein glycosylation. It acts as a lipid carrier of sugars.
Packaging
5 mL Clear Glass Sealed Ampule (900200O-1mg)
5 mL Clear Glass Sealed Ampule (900200O-2mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class
10 - Combustible liquids
wgk
WGK 3
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Dolichol biosynthesis and its effects on the unfolded protein response and abiotic stress resistance in Arabidopsis
Zhang H, et al.
Plant Cell, 20(7), 1879-1898 (2008)
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