Assessing biological variation and protein processing in primary human leukocytes by automated multiplex stable isotope labeling coupled to 2 dimensional peptide separation.
Determining the relative abundances of proteins in biological systems is an important aspect of proteomics. Quantitation provides the possibility to unravel the often subtle molecular differences that regulate biological processes in cells and organisms. A common method to analyze differences in pro...
Main Authors: | Raijmakers, R, Heck, A, Mohammed, S |
---|---|
Formato: | Journal article |
Idioma: | English |
Publicado em: |
2009
|
Registos relacionados
-
Multiplex peptide stable isotope dimethyl labeling for quantitative proteomics.
Por: Boersema, P, et al.
Publicado em: (2009) -
Large Scale Multiplex Stable Isotope Dimethyl Labeling Applied to the Quantitative Analysis of Tyrosine Phosphorylation
Por: Boersema, P, et al.
Publicado em: (2009) -
Applications of stable isotope dimethyl labeling in quantitative proteomics.
Por: Kovanich, D, et al.
Publicado em: (2012) -
Deconvolution of overlapping isotopic clusters improves quantification of stable isotope-labeled peptides.
Por: Cappadona, S, et al.
Publicado em: (2011) -
Fully automated isotopic dimethyl labeling and phosphopeptide enrichment using a microfluidic HPLC phosphochip.
Por: Polat, A, et al.
Publicado em: (2012)