نتایج جستجو برای: preparative electrophoresis

تعداد نتایج: 53897  

2001
Ulrich Groß

Rubisco (Ribulose-1.5-bisphosphate carboxylase/oxygenase) from spinach was purified to homogeneity in one step by gel filtration. This enzyme is suitable for the generation of a specific antibody in rabbits. The enzyme concentration in spinach leaves amounted to 40 % of the total soluble protein. The specific antibody shows cross reaction with crude extracts from leaves of other higher plants. ...

Journal: :Journal of clinical microbiology 1986
G M Carlone M L Thomas H S Rumschlag F O Sottnek

A rapid microprocedure for isolating detergent (sodium N-lauroyl sarcosinate)-insoluble major outer membrane proteins from Haemophilus species produced results qualitatively identical to those obtained with a commonly used preparative isolation procedure. Proteins isolated by both procedures were compared by sodium dodecyl sulfate-polyacrylamide gel electrophoresis after staining with Coomassie...

Journal: :Infection and immunity 1976
M V Lancaster R F Sprouse

Preparative polyacrylamide gel electrophoresis was used to isolate individual components of an alkaline-soluble-water-soluble fraction of the cell wall of Blastomyces dermatitidis yeast phase. One component isolated demonstrated exceptional specificity and reactivity when tested on guinea pigs infected with B. dermatitidis. This component displayed no cross-reactivity when tested on animals inf...

Journal: :Biotechnology and bioengineering 1971
J F Lemp E D Ashbury E O Ridenour

Biological rarticles in liquid suspension exhibit varied electrophoretie mobili:y dependent upon the electric charge behavior of their surface constituents. The surface composition of a population of the same kind of biological particles is uniform in a constant environment. The microscope electrophoresis techniques for mobility and isoelectric point determinations of microscopic particles (bac...

Journal: :Journal of clinical pathology 1971
H N Magnani A N Howard

A rapid, inexpensive, and quantitative method is described for obtaining the levels of plasma very low, low, and high density lipoproteins using cellulose acetate electrophoresis and lipid assays without prior separation by ultracentrifuge or other techniques. It involves separation of the lipoproteins by cellulose acetate electrophoresis, followed by their identification with the ozone-Schiff ...

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