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electrophoresis
(redirected from Two-dimensional gel electrophoresis)

   Also found in: Medical, Acronyms, Encyclopedia, Wikipedia 0.01 sec.
e·lec·tro·pho·re·sis  (-lktr-f-rss)
n.
1. The migration of charged colloidal particles or molecules through a solution under the influence of an applied electric field usually provided by immersed electrodes. Also called cataphoresis.
2. A method of separating substances, especially proteins, and analyzing molecular structure based on the rate of movement of each component in a colloidal suspension while under the influence of an electric field.

e·lectro·pho·retic (-rtk) adj.

electrophoresis [ɪˌlɛktrəʊfəˈriːsɪs]
n
(Chemistry) the motion of charged particles in a colloid under the influence of an applied electric field Also called cataphoresis
electrophoretic  [ɪˌlɛktrəʊfəˈrɛtɪk] adj

electrophoresis  (-lktr-f-rss)
The migration of electrically charged molecules through a fluid or gel under the influence of an electric field. Electrophoresis is used especially to separate combinations of compounds, such as fragments of DNA, for the purpose of studying their components.
ThesaurusLegend:  Synonyms Related Words Antonyms
Noun1.electrophoresis - the motion of charged particles in a colloid under the influence of an electric field; particles with a positive charge go to the cathode and negative to the anode
immunoelectrophoresis - electrophoresis to separate antigens and antibodies
natural action, natural process, action, activity - a process existing in or produced by nature (rather than by the intent of human beings); "the action of natural forces"; "volcanic activity"
carrier electrophoresis, paper electrophoresis - electrophoresis carried out on filter paper


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During the three-day workshop the participants will get hands on training in two-dimensional gel electrophoresis and image processing techniques accompanied with videos and lecture on MDLC, MS etc.
Written for both new and experienced scientists, the text covers two-dimensional gel electrophoresis and protein phosphorylation, enrichment of phosphoproteins and peptides,quantitative analysis of phosphorylation by labeling and MS analysis, antibody and kinase arrays, bioinformatics and phosphosite prediction, identification of phosphoproteins by mass spectrometry, and various chemical tagging strategies.
To identify the possible target proteins of NG in platelets, two-dimensional gel electrophoresis (2-DE)-based comparative proteomics was performed and proteins altered in expressional level after NG treatment were identified by MALDI-TOF MS/MS.
 
 
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