6 Results for "

nonionic surfactant vesicles

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "nonionic surfactant vesicles" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-15435
CAS No.: 75621-03-3
Purity:  99.91%
Research Areas:  

Others

CHAPS is a cholic acid-derived, sulfobetaine-type zwitterionic detergent and micelle-forming agent. CHAPS exhibits properties of weak cationic or nonionic surfactants in different solution systems, undergoes micellization, and forms small, loose hydrophilic aggregates that are temperature-dependent. CHAPS stabilizes mononucleosomes under different ionic strengths, reduces nucleosome sequence specificity, promotes sliding of histone cores along DNA, solubilizes Tamm-Horsfall protein to reduce its interference with urinary exosome isolation, and maintains vesicle structure and the activity of related proteins at the same time. CHAPS is used to recover native folded fusion proteins, enhance the binding capacity of GST fusion proteins, and restore GST enzyme activity. However, CHAPS cannot refold proteins denatured by urea, guanidine hydrochloride or heat, nor can it construct the structure of intrinsically disordered proteins. CHAPS is commonly used in research on the separation and purification of membrane proteins .
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4
4 Cited Publications
Cat. No.: HY-15435A
CAS No.: 331717-45-4
Purity:  ≥98.0%
CHAPS hydrate is a cholic acid-derived, sulfobetaine-type zwitterionic detergent and micelle-forming agent. CHAPS hydrate exhibits properties of weak cationic or nonionic surfactants in different solution systems, undergoes micellization, and forms small, loose hydrophilic aggregates that are temperature-dependent. CHAPS hydrate stabilizes mononucleosomes under different ionic strengths, reduces nucleosome sequence specificity, promotes sliding of histone cores along DNA, solubilizes Tamm‑Horsfall protein to reduce its interference with urinary exosome isolation, and maintains vesicle structure and the activity of related proteins at the same time. CHAPS hydrate is used to recover native folded fusion proteins, enhance the binding capacity of GST fusion proteins, and restore GST enzyme activity. However, CHAPS hydrate cannot refold proteins denatured by urea, guanidine hydrochloride or heat, nor can it construct the structure of intrinsically disordered proteins. CHAPS hydrate is commonly used in research on the separation and purification of membrane proteins .
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Cat. No.: HY-144007
CAS No.: 27321-96-6
Target:  

Liposome

Research Areas:  

Others

Chol-PEG is an amphiphilic cholesterol-polyethylene glycol conjugate and also a liposomelike surface modifier. After Chol-PEG is incorporated into liposomelike vesicles, it forms a hydrophilic barrier on their surface, increases the thickness of the bound water layer around the liposomelike vesicles, and enhances the release rate of encapsulated compounds. Chol-PEG can be used as a modifier to prepare nonionic surfactant vesicles (liposomelike vesicles) for drug delivery applications .
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Cat. No.: HY-W040216
CAS No.: 85261-19-4
Synonyms: N-Nonanoyl-N-methylglucamine
MEGA-9 (N-Nonanoyl-N-methylglucamine) is a green, biodegradable glycosyl nonionic surfactant and micelle-forming agent. MEGA-9 acts as a membrane solubilizer, forms vesicles, solubilizes milk fat, eliminates non-specific reactions of test strips, and restores antigen-antibody reactions in cheddar cheese homogenates for the detection of staphylococcal enterotoxin B (SEB) .
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Cat. No.: HY-W250183C
CAS No.: 9005-00-9
Synonyms: Polyethylene glycol octadecyl ether (n=2)
Research Areas:  

Cancer

Polyoxyethylene (2) stearyl ether (Polyethylene glycol octadecyl ether (n=2)) is a nonionic surfactant. Polyoxyethylene (2) stearyl ether possesses the ability to emulsify, form vesicles, and reverse micelles. Polyoxyethylene (2) stearyl ether is commonly used in biological research such as gene delivery systems and nanovesicle preparation .
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Cat. No.: HY-185564
CAS No.: 118680-70-9
Research Areas:  

Others

F6OM, a nonionic fluorinated octyl maltoside derivative, is a surfactant. F6OM readily interacts with and completely solubilizes phospholipid vesicles via a heterogeneous solubilization mechanism, without compromising membrane order at subsolubilizing concentrations. F6OM promotes bilayer insertion of an integral membrane enzyme in the absence of micelles to support functional refolding of integral membrane proteins. F6OM can be used for membrane-protein applications .
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