نتایج جستجو برای: followed by centrifugation

تعداد نتایج: 7082409  

Journal: :Plant & cell physiology 2008
Yuko Arai Makoto Hayashi Mikio Nishimura

To identify previously unknown peroxisomal proteins, we established an optimized method for isolating highly purified peroxisomes from etiolated soybean cotyledons using Percoll density gradient centrifugation followed by iodixanol density gradient centrifugation. Proteins in highly purified peroxisomes were separated by two-dimensional PAGE. We performed peptide mass fingerprinting of proteins...

Journal: :European Biophysics Journal 2018

Journal: :The Journal of Cell Biology 1974
Christine J. Skerrow A. Gedeon Matoltsy

A method is reported for the isolation of desmosomes in a high yield and of a purity suitable for biochemical analysis. The procedure utilizes the selective solubilizing action of citric acid-sodium citrate (CASC) buffer, pH 2.6, on the non-cornified layers of cow nose epidermis, followed by discontinuous sucrose density gradient centrifugation. Electron microscopy with both thin sections of pe...

Journal: :The Journal of Cell Biology 1982
Y Fujiki A L Hubbard S Fowler P B Lazarow

A rapid and simple method for the isolation of membranes from subcellular organelles is described. The procedure consists of diluting the organelles in ice-cold 100 mM Na2CO3 followed by centrifugation to pellet the membranes. Closed vesicles are converted to open membrane sheets, and content proteins and peripheral membrane proteins are released in soluble form. Here we document the method by ...

Journal: :iranian journal of biotechnology 2014
kamran mousavi hosseini mojgan pourmokhtar mehryar habibi roudkenar majid shahabi

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...

Journal: :Applied and environmental microbiology 1985
H Hirata S Negoro H Okada

By cloning the beta-galactosidase gene of Bacillus stearothermophilus IAM11001 (ATCC 8005) into Bacillus subtilis, enzyme production was enhanced 50 times. beta-Galactosidase could be purified to 80% homogeneity by incubating the cell extract of B. subtilis at 70 degrees C for 15 min, followed by centrifugation to remove the denatured proteins. Because of its heat stability and ease of producti...

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