Protein Chromatography

Author(s):  
Giorgio Carta ◽  
Alois Jungbauer
1987 ◽  
Vol 385 ◽  
pp. 65-74 ◽  
Author(s):  
Timothy D. Schlabach ◽  
Kenneth J. Wilson

2021 ◽  
Author(s):  
Yuanyuan Xia ◽  
Xinping Li ◽  
Yue Yuan ◽  
Jingshun Zhuang ◽  
Wenliang Wang

Abstract The preparation of cellulose beads has attracted more and more attention in the application of advanced green materials. To obtain uniform and controllable cellulose beads, the dissolving pulp was dissolved in NMMO, and the cellulose beads were regenerated in various coagulation baths (water, alcohol, acid, NMMO, etc.) by phase conversion method. Results show that the crystal form of regenerated cellulose changes from cellulose I to cellulose II. NMMO swelling cellulose beads present low crystallinity and low water holding capacity. The coagulation mechanism of cellulose beads was clarified by a laser confocal microscopy. It is found that the whole coagulation process was from outside to inside gradually. It is a green and facile method for preparing cellulose beads with different structures and properties, which can be widely used in biomedicine, energy storage materials, and protein chromatography.


2014 ◽  
Vol 86 (17) ◽  
pp. 8514-8520 ◽  
Author(s):  
Wiebke Mohr ◽  
Tiantian Tang ◽  
Sarah R. Sattin ◽  
Roderick J. Bovee ◽  
Ann Pearson

1977 ◽  
Vol 163 (2) ◽  
pp. 397-400 ◽  
Author(s):  
R J Simmonds ◽  
R J Yon

Human erythrocyte glycophorin was purified rapidly by (a) chromatography of a Triton X-100 extract of erythrocyte ‘ghosts’ on N-(3-carboxypropionyl)aminodecyl-Sepharose in buffers containing Triton X-100 or sodium dodecyl sulphate, or (b) chromatography of whole ‘ghosts’, solubilized in sodium dodecyl sulphate, on dodecyl-Sepharose, in buffers containing sodium dodecyl sulphate. The products contained 85-95% glycophorin (electrophoretic band PAS-1) and the major contaminants were glycoproteins PAS-2 (possibly a subunit of glycophorin) and PAS-3.


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