scholarly journals Chip-Capillary Hybrid Device for Automated Transfer of Sample Preseparated by Capillary Isoelectric Focusing to Parallel Capillary Gel Electrophoresis for Two-Dimensional Protein Separation

2012 ◽  
Vol 84 (16) ◽  
pp. 7001-7007 ◽  
Author(s):  
Joann J. Lu ◽  
Shili Wang ◽  
Guanbin Li ◽  
Wei Wang ◽  
Qiaosheng Pu ◽  
...  
2003 ◽  
Vol 75 (2) ◽  
pp. 215-218 ◽  
Author(s):  
Chun Yang ◽  
Hechun Liu ◽  
Qing Yang ◽  
Lingyi Zhang ◽  
Weibing Zhang ◽  
...  

2014 ◽  
Vol 77 (19-20) ◽  
pp. 1339-1346 ◽  
Author(s):  
Ni Hou ◽  
Yu Chen ◽  
Shiyong Yu ◽  
Zongliang Quan ◽  
Chenhua Pan ◽  
...  

1984 ◽  
Vol 62 (9) ◽  
pp. 847-852 ◽  
Author(s):  
Graham F. Maguire ◽  
J. Alick Little ◽  
Gary Kakis ◽  
W. Carl Breckenridge

Two previously unidentified apolipoproteins (apo) designated apo C-II-X and C-II-Y have been found in plasma of homozygotes and obligate heterozygotes of a family with apo C-II deficiency. Because the plasmas of homozygotes do not activate lipoprotein lipase, apo C-II-X and C-II-Y are apparently nonfunctional. These apolipoproteins have isoelectric focusing points of 5.15 and 5.54, respectively, compared with 4.88 and 4.74 for the known isomorphs, C-II-1 and C-II-2, respectively. They have approximately similar molecular weights to apo C-II-1 and C-II-2 on two-dimensional sodium dodecyl sulphate – glycerol – polyacrylamide slab gel electrophoresis. They do not form insoluble antigen–antibody complexes with antibodies to apo C-II in single antibody immunodiffusion or electroimmunoassay systems. However, using a double-antibody technique in which immunoblotting is coupled with polyacrylamide isoelectric focusing slab gel electrophoresis, apo C-II-1, C-II-2, C-II-X, and C-II-Y have similar reactivity with antibodies to apo C-II. In this family the presence of apo C-II-X and C-II-Y discriminates obligate heterozygotes from normal subjects.


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