scholarly journals A Dataset of Human Liver Proteins Identified by Protein Profiling Via Isotope-coded Affinity Tag (ICAT) and Tandem Mass Spectrometry: Fig. 1.

2004 ◽  
Vol 3 (10) ◽  
pp. 1039-1041 ◽  
Author(s):  
Wei Yan ◽  
Hookeun Lee ◽  
Eric W. Deutsch ◽  
Catherine A. Lazaro ◽  
Weiliang Tang ◽  
...  
2003 ◽  
Vol 2 (7) ◽  
pp. 426-427 ◽  
Author(s):  
Priska D. von Haller ◽  
Eugene Yi ◽  
Samuel Donohoe ◽  
Kelly Vaughn ◽  
Andrew Keller ◽  
...  

2003 ◽  
Vol 2 (7) ◽  
pp. 428-442 ◽  
Author(s):  
Priska D. von Haller ◽  
Eugene Yi ◽  
Samuel Donohoe ◽  
Kelly Vaughn ◽  
Andrew Keller ◽  
...  

2006 ◽  
Vol 8 (4) ◽  
pp. 513-520 ◽  
Author(s):  
Cecily P. Vaughn ◽  
David K. Crockett ◽  
Megan S. Lim ◽  
Kojo S.J. Elenitoba-Johnson

Author(s):  
Jose Chou ◽  
Pankaj Choudhary ◽  
Steven Goodman

AbstractA proteomic approach using a cleavable ICAT reagent and nano-LC ESI tandem mass spectrometry was used to perform protein profiling of core RBC membrane skeleton proteins between sickle cell patients (SS) and controls (AA), and determine the efficacy of this technology. The data was validated through Peptide/Protein Prophet and protein ratios were calculated through ASAPratio. Through an ANOVA test, it was determined that there is no significant difference in the mean ratios from control populations (AA1/AA2) and sickle cell versus control populations (AA/SS). The mean ratios were not significantly different from 1.0 in either comparison for the core skeleton proteins (α spectrin, β spectrin, band 4.1 and actin). On the natural-log scale, the variation (standard deviation) of the method was determined to be 14.1% and the variation contributed by the samples was 13.8% which together give a total variation of 19.7% in the ratios.


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