产品名称
NP-40 Alternative, PROTEIN GRADE® Detergent, 10% Solution, Sterile-Filtered, A non-ionic surfactant useful for the isolation and purification of functional membrane protein complexes. This detergent has been purified to reduce levels of contaminating aldehydes, metals, peroxides, and salts.
SMILES string
O(CCOc1ccc(cc1)CCCCCCCCC)CCO
InChI
1S/C19H32O3/c1-2-3-4-5-6-7-8-9-18-10-12-19(13-11-18)22-17-16-21-15-14-20/h10-13,20H,2-9,14-17H2,1H3
InChI key
BLXVTZPGEOGTGG-UHFFFAOYSA-N
description
RTECS - MD0905000
product line
Calbiochem®
form
solution
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
impurities
≤200 μM Aldehyde
≤200 μM peroxide
color
clear colorless
conductivity
≤50 μmho
CMC
50 - 300 μM
solubility
water: soluble
application(s)
(Isolating membrane proteins)
shipped in
ambient
storage temp.
2-8°C
Quality Level
Disclaimer
Toxicity: Irritant (B)
General description
A non-ionic surfactant used in the isolation and purification of functional membrane protein complexes and in two-dimensional gel electrophoresis (2DGE). Similar in usage to NP-40 and TRITON™ X-100 (Cat. No. 648462). Purified to reduce levels of contaminating aldehydes, metals, peroxides, and salts. CMC: 50-300 µM.
A non-ionic surfactant useful for the isolation and purification of functional membrane protein complexes. This detergent has been purified to reduce levels of contaminating aldehydes, metals, peroxides, and salts.
Other Notes
Ripoche, P., et al. 1982. Biochim. Biophys. Acta693, 497.
Physical form
10% aqueous solution.
Preparation Note
Following initial use, aliquot and freeze (-20°C).
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
PROTEIN GRADE is a registered trademark of Merck KGaA, Darmstadt, Germany
Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 3
法规信息
监管及禁止进口产品
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Whereas folding of genomes at the large scale of epigenomic compartments and topologically associating domains (TADs) is now relatively well understood, how chromatin is folded at finer scales remains largely unexplored in mammals. Here, we overcome some limitations of conventional
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