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1 In this paper we characterize the tyrosine-phosphorylated proteins by two- dimensional gel electrophoresis.
2 Cell extracts of this line were prepared and subjected to two- dimensional gel electrophoresis.
3 The expression of proteins was visualized by silver stain after two- dimensional gel electrophoresis.
4 Here we report the development of a two- dimensional gel electrophoresis database of lysosomal proteins.
5 Using two- dimensional gel electrophoresis we compared the protein expression profiles of both groups of livers.
6 Serum proteome profiles were created by two- dimensional gel electrophoresis.
7 It was detected 4 hrs after irradiation by two dimensional gel electrophoresis and silver staining.
8 The new concept of 'normalized virtual one- dimensional gel ' is introduced, making comparisons between gels particularly easy.
9 A one- dimensional gel analysis method is then described.
10 Two- dimensional gel electrophoresis, Western blot, and mass spectroscopy were also performed to identify S100a and other proteins.
11 The protein extracts were obtained from 18 separate mussel samples and were analyzed by two- dimensional gel electrophoresis.
12 Two- dimensional gel electrophoresis resolved more than 1,000 protein spots on each gel.
13 The proteins in the cerebral cortex were separated using two- dimensional gel electrophoresis and were identified by mass spectrometry.
14 To identify protective antigens, whole cell proteome of C. botulinum type B was separated by two- dimensional gel electrophoresis.
15 The two- dimensional gel electrophoresis profiles of the fractions were analyzed and automatically compared by the computer system MELANIE.
16 A comparison of the various methods disclosed the one- dimensional gel - LC and the shaving approach to be highly complementary techniques.
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This collocation consists of: Dimensional gel through the time
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