missing translation for 'onlineSavingsMsg'
Learn More

Thermo Scientific™ Tween™ 80 Surfact-Amps™ Detergent Solution

Catalog No. PI28329
Change view
Click to view available options
Quantity:
50 mL
500 mL
6 x 10 mL
3 product options available for selection
Product selection table with 3 available options. Use arrow keys to navigate and Enter or Space to select.
Catalog No. Quantity
PI28329 50 mL
PI28328 6 x 10 mL
PI28230 500 mL
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 3 options available.
3 options
Catalog No. PI28329 Supplier Thermo Scientific™ Supplier No. LSG28329
Only null left

Thermo Scientific™ Surfact-Amps 80 Detergent Solution is highly-purified Tween-80 detergent stabilized and supplied as a 10% solution in 10mL glass ampules.

Thermo Scientific™ Tween-80 Detergent Surfact-Amps™ Solution is highly-purified Tween-80 detergent stabilized and supplied as a 10% solution in 10mL glass ampules.

This is an easy-to-use 10% (w/v) solution of purified Tween-80 detergent for use in routine and high-demand protein research methods and molecular biology techniques. Tween-80 is a nonionic polyoxyethylene surfactant that is most frequently added to PBS or TBS wash buffers for ELISA, Western blotting and other immunoassay methods.

Surfact-Amps™ Detergent Solutions (10% w/v) provide unsurpassed purity, quality and stability. Unlike neat detergents, which are extremely viscous, Surfact-Amps 10% Solutions are easy to pipette and accurately dispense. The surfactant solutions are carefully prepared and packaged under nitrogen in glass ampules, ensuring their stability and eliminating the accumulation of peroxides and degradation products.

Highlights:

Tween 80 – a nonionic detergent for use in wash buffers

Accurate – precise 10% detergent solution in ultrapure water

Easy-to-use – solution is simple to dispense and dilute for use

Exceptionally pure – less than 1.0μeq/ml peroxides and carbonyls

Stable – packed in glass ampules under inert nitrogen gas

Detergent Properties:

  • Molecular Weight: 1310
  • Detergent Class: Nonionic
  • Aggregation Number: 60
  • Micelle Molecular Weight: 76,000
  • Critical Micelle Concentration (CMC): 0.012mM (0.0016%, w/v)
  • Cloud Point: Unknown
  • Dialyzable: No

Specifications

Product Type Detergent
Content And Storage Store in a cool, dry, and well-ventilated area
Form Liquid
Product Line Surfact-Amps, Tween
Reagent Type Detergent Solution
Quantity 50 mL
What are the main advantages of using Thermo Scientific Pierce Surfact-Amps detergents?

Thermo Scientific Pierce Surfact-Amps detergents are highly purified, precisely diluted (10%) formulations that are ideal for applications or assays that are sensitive to contaminants that are present in unpurified detergents. We test every batch to insure that our detergents contain less than 1.0 µeq/mL peroxides and carbonyls and package them under nitrogen, to prevent oxidization during storage.

Superior quality - lower measurable contaminant levels than other leading vendors
Accurate -precise 10% detergent solution in ultrapure water
Easy-to-use - solution is simple to dispense and dilute for use
Exceptionally pure - less than 1.0 µeq/mL peroxides and carbonyls

Are detergents denaturing or non-denaturing with respect to protein structure?

Ionic detergents, or those that carry a charge, are the most likely to be denaturing to proteins. Denaturing detergents can be anionic such as sodium dodecyl sulfate (SDS) or cationic such as ethyl trimethyl ammonium bromide. These detergents totally disrupt membranes and denature proteins by breaking protein-protein interactions through changes in the three-dimensional structure of the proteins. Nondenaturing detergents can be divided into nonionic detergents (i.e., Triton X-100), bile salts (i.e., cholate), and zwitterionic detergents (i.e., CHAPS).

What are detergents?

Detergents are amphipathic molecules containing both a nonpolar “tail” having aliphatic or aromatic character, and a polar “head”. The ionic character of the polar head group forms the basis for broad classification of detergents as ionic, nonionic, or zwitterionic.

How does detergent-based cell lysis work?

Detergents are amphipathic molecules, meaning they contain both a nonpolar “tail” having aliphatic or aromatic character and a polar “head”. Like the components of biological membranes, detergents have hydrophobic-associating properties as a result of their nonpolar tail groups. Nevertheless, detergents are themselves water soluble.

Consequently, detergent molecules allow the dispersion (miscibility) of water-insoluble, hydrophobic compounds into aqueous media, including the extraction and solubilization of membrane proteins. Detergent monomers solubilize membrane proteins by partitioning into the membrane bilayer. With increasing amounts of detergents, membranes undergo various stages of solubilization.

What types of detergents are available for cell lysis?

Detergents can be denaturing or non-denaturing with respect to protein structure. Denaturing detergents can be anionic such as sodium dodecyl sulfate (SDS) or cationic such as ethyl trimethyl ammonium bromide. These detergents totally disrupt membranes and denature proteins by breaking proteinprotein interaction. These detergents are considered harsh. Non-denaturing detergents can be divided into nonionic detergents (i.e., Triton X-100), bile salts (i.e., cholate), and zwitterionic detergents (i.e., CHAPS). These detergents do not denature proteins and do not break protein-protein interactions. These detergents are considered mild.

Why does the method of cell lysis matter?

Cell lysis is the first step in cell fractionation, organelle isolation, and protein extraction and purification. As such, cell lysis opens the door to a myriad of proteomics research methods. Many techniques have been developed and used to obtain the best possible yield and purity for different species of organisms, sample types (cells or tissue), and target molecule or subcellular structure. Subcellular fractionation and protein enrichment are important methods in the rapidly growing field of proteomics. Isolation of subcellular fractions and concentration of proteins in low abundance allow for more efficient identification and study of proteins of interest. Examples are the isolation of integral membrane proteins and nuclear proteins.

What methods of cell lysis are available?

Historically, physical lysis was the method of choice for cell disruption and extraction of cellular contents; however, it often requires expensive, cumbersome equipment and involves protocols that can be difficult to repeat due to variability in the apparatus (such as loose-fitting compared with tight-fitting homogenization pestles). Also, traditional physical disruption methods are not conducive for high-throughput and smaller volumes typical of modern laboratory research.
In recent years, detergent-based cell lysis methods have become the norm. Through empirical testing by trial and error, different detergent-based solutions composed of particular types and concentrations of detergents, buffers, salts and reducing agents have been developed to provide the best possible results for particular species and types of cells. Detergents have both lysing and solubilizing effects.


For Research Use Only. Not for use in diagnostic procedures.