نتایج جستجو برای: linking reagents

تعداد نتایج: 91438  

Journal: :jundishapur journal of natural pharmaceutical products 0
jebraeel movaffagh targeted drug delivery research center, department of pharmaceutics, school of pharmacy, mashhad university of medical sciences, ir iran ali ghodsi targeted drug delivery research center, department of pharmaceutics, school of pharmacy, mashhad university of medical sciences, ir iran bibi sedigheh fazly bazzaz biotechnology research center, school of pharmacy, mashhad university of medical sciences, ir iran sayyed abolghassem sajadi tabassi targeted drug delivery research center, department of pharmaceutics, school of pharmacy, mashhad university of medical sciences, ir iran; pharmacological research center of medicinal plants, school of medicine, mashhad university of medical sciences, ir iran +98-5118823255, [email protected]; pharmacological research center of medicinal plants, school of medicine, mashhad university of medical sciences, ir iran +98-5118823255, [email protected] hamideh ghodrati azadi department of basic sciences, fcaulty of veterinary medicine, ferdowsi university of mashhad, ir iran

background chitosan is a naturally occurring biopolymer which has been widely used in a variety of biomedical applications including local antibiotic delivery due to its excellent mechanical properties, biodegradability and biocompatibility. beads are spherical, porous carriers which are prepared from various materials including chitosan. objectives the current study aimed to fabricate a new co...

Journal: :Bioscience reports 2001
K N Myasoedova N N Magretova

Proteoliposomes, containing cytochrome P450 1A2, were obtained by the cholate-dialysis technique. The effect of bifunctional cross-linking reagents on the purified hexameric cytochrome P450 1A2 in an aqueous medium and on the proteoliposomal P450 1A2 have been compared. Electrophoretic analysis of the modified proteins demonstrated the same oligomeric (hexameric) organization of the hemoprotein...

Journal: :Journal of the American Chemical Society 2003
Michelle Trester-Zedlitz Katsuhiko Kamada Stephen K Burley David Fenyö Brian T Chait Tom W Muir

A method is described for the elucidation of protein-protein interactions using novel cross-linking reagents and mass spectrometry. The method incorporates (1) a modular solid-phase synthetic strategy for generating the cross-linking reagents, (2) enrichment and digestion of cross-linked proteins using microconcentrators, (3) mass spectrometric analysis of cross-linked peptides, and (4) compreh...

Journal: :The Journal of biological chemistry 1976
R B Mikkelsen D F Wallach

We describe the reactions of three lipophilic, photoactivated cross-linking reagents, 1,5-diazidonapthalene, 4,4'-diazidobiphenyl, and the reversible 4,4'-dithiobisphenylazide, with erythrocyte membranes. Cross-linking occurs only upon photoactivation. At pH 7 to 8, only spectrin components are cross-linked by these reagents. At pH 5.0 to 5.5 several additional membrane proteins including the m...

Techniques of immobilization of microbial- cells have been established by multifunctional reagents such as glutaraldehyed on a solid support. Immobilized cell reactor was designed to demonstrate stability of cross linking of whole cells for the production of organic acids. An eighty-six percent conversion of glucose was obtained for an eight hour retention time. The immobilized cell reacto...

Journal: :Bioconjugate chemistry 1998
J Ottl D Gabriel G Marriott

The design, synthesis, and spectroscopic and chemical properties of four members of a new class of heterobifunctional photocleavable (caged) cross-linking reagents were described. One of the two reactive groups of the cross-linker reacted with amino groups to form the corresponding photolabile carbamates. Amino group containing compounds or proteins caged with these reagents can be coupled thro...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1971
S S Husain J B Ferguson J S Fruton

Two bifunctional reagents designed to probe the active site of pepsin and other acid proteinases are described. One of these, the bisdiazoketone 1,1-bis(diazoacetyl)-2-phenylethane inactivates pepsin at pH 5.0 much more rapidly than the corresponding monodiazoketon 1-diazoacetyl-2-phenylethane, whereas the other, the bromodiazoketone dl-1-diazoacetyl-1-bromo-2-phenylethane is less effective in ...

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