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O3757

Sigma-Aldrich

Octyl β-D-glucopyranoside solution

≥95% (HPLC), 50 % (w/v) in H2O

Sinónimos:

n-Octyl glucoside, OGP

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About This Item

Fórmula empírica (notación de Hill):
C14H28O6
Número de CAS:
29836-26-8
Peso molecular:
292.37
MDL number:
MFCD00063288
UNSPSC Code:
12161902
PubChem Substance ID:
24897986
NACRES:
NB.22

description

non-ionic

Quality Level

200

assay

≥95% (HPLC)

mol wt

average mol wt 24500-25000

concentration

50 % (w/v) in H2O

aggregation number

84

CMC

20-25

transition temp

cloud point ≥100

application(s)

detection

storage temp.

−20°C

SMILES string

CCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI

1S/C14H28O6/c1-2-3-4-5-6-7-8-19-14-13(18)12(17)11(16)10(9-15)20-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1

InChI key

HEGSGKPQLMEBJL-RKQHYHRCSA-N

Application

2.5% n-octyl β-D glucopyranoside has been used to homogenize mouse retina
n-Octyl β-D-glucopyranoside (OGP) is a non-ionic detergent which has been used for isoelectric focusing (IEF) and two-dimensional electrophoresis (2D). OGP has been shown to be superior to Triton™ X-100 for IEF of plant proteins. n-Octyl β-D-glucopyranoside has also been used for concentration of protein from 2D gels for digestion and mass spectroscopy analysis.

Legal Information

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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P Dainese Hatt et al.
European journal of biochemistry, 246(2), 336-343 (1997-06-01)
We have developed a gel electrophoresis system that can concentrate proteins from spots cut out of up to 50 two-dimensional electrophoresis gels. During protein concentration, SDS is substituted with a non-ionic detergent (octyl beta-glucopyranoside) which allows digestion and MS analysis
P J Holloway et al.
Analytical biochemistry, 172(1), 8-15 (1988-07-01)
A technique for the analysis of plant proteins from seed, leaf, root, and coleoptile tissues by high resolution two-dimensional electrophoresis is described. This technique is based primarily on the procedure of P. O'Farrell (1975, J. Biol. Chem. 250, 4007-4021); however
M F Lopez
Journal of chromatography. B, Biomedical sciences and applications, 722(1-2), 191-202 (1999-03-06)
Two-dimensional electrophoresis has rapidly become the method of choice for resolving complex mixtures of proteins. Since the technique was pioneered in 1975, 2-D gel methods have undergone a series of enhancements to optimize resolution and reproducibility. Recent improvements in the
Compartment-specific phosphorylation of phosducin in rods underlies adaptation to various levels of illumination.
Song H, et al.
The Journal of Biological Chemistry (2007)
Chaoqun Yao et al.
Proteomics. Clinical applications, 4(1), 4-16 (2010-12-08)
About two million new cases of leishmaniasis with 50 000 associated deaths occur worldwide each year. Promastigotes of the causative Leishmania spp. develop from the procyclic stage to the highly virulent metacyclic stage within the sand fly vector. We hypothesized
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