نتایج جستجو برای: crude protein fractionation

تعداد نتایج: 1277498  

Kamran Mousavi Hosseini, Majid Shahabi Mehryar Habibi Roudkenar Mojgan Pourmokhtar

Background: There are varieties of purification techniques for separation of human plasma proteins such as salting out, ion exchange chromatography, and ethanol fractionation. There are limitations for each method, for example in salting out method, the salt has to be removed in an additional step. Ion exchange chromatography is difficult for scaling up, and plasma fractionation is a time consu...

2000
John J. Chung Lal A. Ratnapala Ian M. Cooke Angel A. Yanagihara

We have isolated and characterized a novel hemolytic protein from the venom of the Hawaiian box jelly®sh (Carybdea alata). Hemolysis of sheep red blood cells was used to quantitate hemolytic potency of crude venom extracted from isolated nematocysts and venom after fractionation and puri®cation procedures. Hemolytic activity of crude venom was reduced or lost after exposure to the proteolytic e...

BAHMAN TABARAIE, FERESHTEH SHAHCHERAGHI, GHORBAN BEHZADIAN-NEJAD, MOHAMMAD BAGHER ESLAMI,

Isolation and purification of major outer membrane proteins (OMP) from the cell wall envelope of Brucella abortus S-99 were achieved by sonication, solubilization and membrane fractionation in the presence of non-ionic detergent (Tx-100) and lysozyme treatments, followed by ultracentrifugation. The crude OMP was treated with trypsin to free the preparation from any other protein contaminan...

Journal: :The Journal of biological chemistry 1951
P S CAMMARATA P P COHEN

Because of the general nature of the transamination reaction (1, 2), a study of the kinetics and mechanism of reaction seemed of interest. Preliminary studies of this nature have already appeared (3-5). However, these studies were carried out with crude extracts or resolved enzyme systems. In order to conduct a critical kinetic study as well as a study of the mechanism of reaction, large amount...

Journal: :medical journal of islamic republic of iran 0
fereshteh shahcheraghi from the department of microbiology, medical school, tarbiat modaress university, tehran, mohammad bagher eslami from the department of microbiology, medical school, tarbiat modaress university, tehran, bahman tabaraie the department of bacterial vaccine and antigen production, pasteur institute of iran, tehran, islamic republic of iran. ghorban behzadian-nejad from the department of microbiology, medical school, tarbiat modaress university, tehran,

isolation and purification of major outer membrane proteins (omp) from the cell wall envelope of brucella abortus s-99 were achieved by sonication, solubilization and membrane fractionation in the presence of non-ionic detergent (tx-100) and lysozyme treatments, followed by ultracentrifugation. the crude omp was treated with trypsin to free the preparation from any other protein contaminants. t...

A. Matinfar M.H. Abolhasani R. Ghorbani R. Ghorbani Vaghei, Sh. Dadgar

Advantages of pelleted feeds in terms of storage, transportation and lower costs compared to natural fresh feed justified the replacement of artificial feeds instead of natural ones partially on maturation performances. This study comprised nine treatments (with three replications) including control treatment: polychaete worm (Perinereis nuntia), Squid and calf liver (natural feed); T1: pellet ...

Journal: :The Journal of biological chemistry 1968
P F Bartell G K Lam T E Orr

A polysaccharide depolymerase was puritied 1,688-fold from crude lysates produced by the propagation of a specitic bacteriophage in Pseudomonas aeruginosa. Conventional methods of protein fractionation were employed, namely, salting out with ammonium sulfate, Sephadex gel filtration, and high speed centrifugation. The purified depolymerase behaves as a single entity when tested by electrophores...

1990
P. F. BARTELL

A polysaccharide depolymerase was puritied 1,688-fold from crude lysates produced by the propagation of a specitic bacteriophage in Pseudomonas aeruginosa. Conventional methods of protein fractionation were employed, namely, salting out with ammonium sulfate, Sephadex gel filtration, and high speed centrifugation. The purified depolymerase behaves as a single entity when tested by electrophores...

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