Electrophoresis is the main metod for separating large polyelectrolyte molecules, primarily used on DNA, in biochemistry and medicine research. An overwiev of the models of physical mechanisms that are behind this phenomena will be presented. The prominent role is taken by reptation mechanisms, by which large ‡exible polyelectrolytes thread their way through the pores of the gel matrix. There a...

The separation of polypeptides by electrophoresis allowed Arne Tiselius to describe protein fractions corresponding to albumin, -, -, and -globulins in serum with the Rrst published diagram of human serum protein electrophoresis in 1939. The number of fractions slowly expanded into electrophoretic subfractions identiRed as 1, 2, 1, 2, 1 and 2. The mobility characteristics of these fractions are...

The discovery that antigen}antibody interaction could be produced not only in liquids, but also on gel media, such as agar or agarose gels, with the formation of insoluble immunoprecipitates, opened the door to the development of the gel diffusion techniques for immunoprecipitation analysis. The Rrst of these techniques, known as double diffusion, was introduced by Ouchterlony in 1948. In this ...

Curli are extracellular amyloid fibres produced by Escherichia coli that are critical for biofilm formation and adhesion to biotic and abiotic surfaces. CsgA and CsgB are the major and minor curli subunits, respectively, while CsgE, CsgF and CsgG direct the extracellular localization and assembly of curli subunits into fibres. The secretion and stability of CsgA and CsgB are dependent on the ou...

results the results showed that nl1-gc/ls2 primer set could yield species-specific amplicons, which were well distinguished and allowed better species discrimination than that generated by the its3-gc/its4 primer set, in both dgge and ttge profiles. all five candida species were discriminated by dgge and ttge using the nl1-gc/ls2 primer set. conclusions comparison of dgge and ttge profiles obta...

The most common technique for sorting, identifying, and purifying nucleic acid fragments is agarose gel electrophoresis. performance of the electrophoresis could be impacted by buffers’ composition, ionic strength, pH characteristics [1].