نتایج جستجو برای: exchange chromatography

تعداد نتایج: 289840  

Journal: :journal of medical bacteriology 0
ehsan zayerzadeh department of biology, faculty of food industry and agriculture, standard research institute, karaj, ir iran. azadeh fardipour department of vaccine quality control, razi vaccine and serum research institute, karaj, ir iran. ahmadreza jabbari department of anaerobic bacterial vaccine research & production, razi vaccine and serum research institute, karaj, ir iran.

background : clostridium perfringens type c strains cause severe necrotizing enteritis in sheep, calves, goats, pigs and humans. beta-toxin is introduced to be the essential virulence factor of this microorganism. in the present study, a new method was established for the purification of beta toxin from culture supernatant fluid of c. perfringens type c vaccinal strain. methods : the four steps...

Journal: :Indian journal of biochemistry & biophysics 1999
V Singh R C Singh R K Dubey A Alam

Gelonin, a ribosome-inactivating protein has been isolated from the seeds of Gelonium multifluorum of Euphorbiaceae family by two methods and the results are compared. In method-I conventional aqueous extraction, cation-exchange and gel-filtration chromatography has been used. In method-II S-Sepharose fast flow gel has been used to purify the proteins from the seed extract, followed by ammonium...

Journal: :Acta Crystallographica Section D Structural Biology 2016

Journal: :Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie 1985
L Siekmann

A method for the measurement of uric acid in human serum by isotope dilution-mass spectrometry is described. The analytical procedure consists of the following steps: Addition of [1,3-15N2]uric acid to the serum sample; ion exchange chromatography on AG1-X2; formation of the trimethylsilyl derivative; gas liquid chromatography-mass spectrometry (GC-MS), selected ion monitoring (SIM) at m/z-valu...

Journal: :Clinical chemistry 1990
M Grøstad R Rej N E Huseby

We describe an improved separation of the isoenzymes of aspartate aminotransferase (EC 2.6.1.1), based on ion-exchange chromatography. Involving the "Fast Protein Liquid Chromatography" system (Pharmacia) with a MonoQ column, this rapid, reproducible method for quantifying the mitochondrial enzyme shows good resolution and sensitivity, and results correlate well with those by an established imm...

Journal: :Bioscience, biotechnology, and biochemistry 1999
C H Pan E A Lee Y A Chae S I Kim

We have purified a 21-kDa protein, designated as P1, from Rehmannia glutinosa to homogeneity by ammonium sulfate precipitation, anion exchange chromatography, hydrophobic interaction chromatography, and preparative native PAGE. The purified P1 had chitin degradation activity. The N-terminal amino acid sequence of P1 indicated that it is very similar to those of thaumatin and other reported thau...

Journal: :The Biochemical journal 1967
M C Corfield J C Fletcher A Robson

1. A tryptic digest of the protein fraction U.S.3 from oxidized wool has been separated into 32 peptide fractions by cation-exchange resin chromatography. 2. Most of these fractions have been resolved into their component peptides by a combination of the techniques of cation-exchange resin chromatography, paper chromatography and paper electrophoresis. 3. The amino acid compositions of 58 of th...

Journal: :Indian journal of biochemistry & biophysics 2013
Li-Jing Xu Qing-Jun Chen He-Xiang Wang Guo-Qing Zhang

A 15 kDa ribonuclease (RNase) was purified from dried fruiting bodies of the wild edible mushroom Armillaria luteo-virens. The simple 4-step purification protocol involved ion-exchange chromatography on DEAE-cellulose, affinity chromatography on Affi-gel blue gel, ion-exchange chromatography on SP-Sepharose and a final gel filtration by FPLC on Superdex-75. The RNase was unadsorbed on Affi-gel ...

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