67228
Poly(maleic anhydride-alt-1-decene), 3-(dimethylamino)-1-propylamine derivative
BioReagent, for molecular biology
Synonym(s):
PMAL®-C8
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![Poly[(isobutylene-alt-maleic acid, ammonium salt)-co-(isobutylene-alt-maleic anhydride)] average Mw ~60,000](/deepweb/assets/sigmaaldrich/product/structures/208/717/cfb2dcac-b112-4e25-9140-f3649ec430ea/640/cfb2dcac-b112-4e25-9140-f3649ec430ea.png)
biological source
synthetic
grade
Molecular Biology
for molecular biology
description
zwitterionic
product line
BioReagent
color
white to off-white
λ
0.1 % in H2O
UV absorption
λ: 260 nm Amax: ≤0.550
λ: 280 nm Amax: ≤0.200
application(s)
hematology
histology
storage temp.
room temp
Analysis Note
enzyme traces DNases, RNases, proteases and phosphatases not detectable
Legal Information
PMAL is a registered trademark of Affymetrix, Inc.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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J K Nagy et al.
FEBS letters, 501(2-3), 115-120 (2001-07-27)
Data are presented which suggest that a class of amphiphilic polymers known as 'amphipols' may serve as a vehicle for delivering complex integral membrane proteins into membranes. The integral membrane protein diacylglycerol kinase (DAGK) was maintained in soluble form by
Bonnie M Gorzelle et al.
Journal of the American Chemical Society, 124(39), 11594-11595 (2002-09-26)
Amphipathic polymers ("amphipols") were introduced several years ago (Tribet, C.; Audebert, R.; Popot, J.-L. Proc. Natl. Acad. Sci. U.S.A. 1996, 93, 15047-15050) as an alternative method for solubilizing integral membrane proteins in stable, nativelike conformations. However, direct maintenance of full
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