282103
Triton™ X-100 reduced
Synonyme(s) :
Polyoxyethylene (10) isooctylcyclohexyl ether
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A propos de cet article
Formule linéaire :
4-(C8H17)C6H10(OCH2CH2)nOH, n~10
Numéro CAS:
UNSPSC Code:
12162002
NACRES:
NA.23
MDL number:
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Laissez-nous vous aiderInChI
1S/C28H56O8/c1-27(2,3)24-28(4,5)25-6-8-26(9-7-25)36-23-22-35-21-20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29/h25-26,29H,6-24H2,1-5H3
SMILES string
CC(C)(C)CC(C)(C)C1CCC(CC1)OCCOCCOCCOCCOCCOCCOCCO
InChI key
QQJNBKDKLMCALZ-UHFFFAOYSA-N
refractive index
n20/D 1.473 (lit.)
density
1.029 g/mL at 25 °C (lit.)
Quality Level
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Catégories apparentées
General description
Triton™ X-100 reduced (RTX-100) is formed when the benzene moiety of TX-100 is fully hydrogenated to a cyclohexane derivative. RTX-100 might enhance enzyme digestion and is also known to exhibit some effects on the photoisomerization of bacteriorhodopsin.
Triton™ X-100 reduced is a versatile nonionic surfactant with a hydrophilic polyethylene oxide chain, widely utilized as a laboratory detergent. Its applications span various areas, including cell biology and biochemical research. This detergent is commonly employed for tasks such as cell lysis to extract proteins or organelles, permeabilizing the membranes of living cells, and serving as a crucial component in lysis buffers. Triton™ X-100 plays a key role in the isolation of lipid rafts, contributing to enhanced solubility and dispersibility of substances. With a reduced polyoxyethylene content of approximately 10, Triton™ X-100 exhibits excellent wetting properties and facilitates emulsification.
In biochemical and cell biology research, Triton™ X-100 is instrumental in solubilizing membrane-bound proteins and isolating lipid rafts. Its unique properties allow for the preservation of the native conformation of proteins obtained from cellular membranes in solution. Triton™ X-100 reduced is derived from the full hydrogenation of the benzene moiety of TX-100 to a cyclohexane derivative. This modified version, RTX-100, has demonstrated potential in enhancing enzyme digestion and influencing the photoisomerization of bacteriorhodopsin, showcasing its versatility and utility in advanced research applications.
In biochemical and cell biology research, Triton™ X-100 is instrumental in solubilizing membrane-bound proteins and isolating lipid rafts. Its unique properties allow for the preservation of the native conformation of proteins obtained from cellular membranes in solution. Triton™ X-100 reduced is derived from the full hydrogenation of the benzene moiety of TX-100 to a cyclohexane derivative. This modified version, RTX-100, has demonstrated potential in enhancing enzyme digestion and influencing the photoisomerization of bacteriorhodopsin, showcasing its versatility and utility in advanced research applications.
Application
Triton™ X-100 reduced has been used:
- as a component of LB-TT for the extraction of total protein from rat brains
- in ADP-Glo assay and Cytophos adenosine triphosphatase (ATPase) assay
- in phosphate-buffered saline (PBS) solution for the permeabilization of fibroblasts in 5′ ethynyl uridine staining, immunofluorescence, and immunolabeling
Features and Benefits
- Non-ionic surfactant
- Reduced polyoxyethylene content (~10)
- Improves solubility and dispersibility of substances
- Excellent wetting properties
- Enhances emulsification
- High purity product for research applications
Other Notes
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Legal Information
Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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J Fernandez et al.
Analytical biochemistry, 218(1), 112-117 (1994-04-01)
An improved and simplified procedure for enzymatic digestion of proteins bound to polyvinylidene difluoride (PVDF) membranes for obtaining internal protein sequence data is presented. This improved procedure is compatible with various enzymes (trypsin, endoproteinase Lys-C, endoproteinase Glu-C, and clostripain) and
S J Milder et al.
Biochemistry, 30(7), 1751-1761 (1991-02-19)
Time-resolved difference spectra have been obtained for the photocycle of delipidated bacteriorhodopsin monomers (d-BR) in six different detergent micelle environments that were prepared by two new detergent-exchange techniques. A global kinetic analysis of the photocycle spectra for d-BR in each
Yoshinori Masuo et al.
Methods in molecular biology (Clifton, N.J.), 829, 505-530 (2012-01-11)
Mechanisms underlying behavioral abnormalities of patients with attention-deficit hyperactivity disorder (ADHD) disorder are still unknown. It is worth clarifying alterations in the brain of animal models for ADHD. The animals with neonatal treatment with 6-hydroxydopamine (6-OHDA) and congenic wiggling (Wig)
Electrodilatometry 5: Triton X-100 (reduced form) in cyclohexane
Rappon M and Lin SE
Journal of Molecular Liquids, 116(3), 125-130 (2005)
Andrew G Reidenbach et al.
Cell chemical biology, 25(2), 154-165 (2017-12-05)
Human COQ8A (ADCK3) and Saccharomyces cerevisiae Coq8p (collectively COQ8) are UbiB family proteins essential for mitochondrial coenzyme Q (CoQ) biosynthesis. However, the biochemical activity of COQ8 and its direct role in CoQ production remain unclear, in part due to lack
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