共 73 条
Relative quantification in proteomics: new approaches for biochemistry
被引:42
作者:

Unwin, Richard D.
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机构:
Univ Manchester, Stem Cell & Leukaemia Prot Lab, Manchester M20 4QL, Lancs, England Univ Manchester, Stem Cell & Leukaemia Prot Lab, Manchester M20 4QL, Lancs, England

Evans, Caroline A.
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机构:
Univ Manchester, Stem Cell & Leukaemia Prot Lab, Manchester M20 4QL, Lancs, England Univ Manchester, Stem Cell & Leukaemia Prot Lab, Manchester M20 4QL, Lancs, England

Whetton, Anthony D.
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机构:
Univ Manchester, Stem Cell & Leukaemia Prot Lab, Manchester M20 4QL, Lancs, England Univ Manchester, Stem Cell & Leukaemia Prot Lab, Manchester M20 4QL, Lancs, England
机构:
[1] Univ Manchester, Stem Cell & Leukaemia Prot Lab, Manchester M20 4QL, Lancs, England
基金:
英国生物技术与生命科学研究理事会;
关键词:
D O I:
10.1016/j.tibs.2006.06.003
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Recent developments in mass spectrometry and protein arrays provide opportunities to derive systematically proteomic information from small samples of cellular material. Relative quantification among samples can be achieved with either gel-based or gel-free approaches. Furthermore, the adaptation of specific techniques facilitates absolute quantification. Here, relative quantification in two-dimensional gel electrophoresis is contrasted with that in non-gel-based approaches such as isobaric tagging of peptides, pre-labelling of living cells with isotopomeric forms of essential amino acids and protein array platforms. In addition, novel flow cytometry-based approaches are considered. These technologies can all be used to determine accurately the levels of proteins or biomarkers in a wide range of samples.
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收藏
页码:473 / 484
页数:12
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