Vermel electrophoresis - translation to ρωσικά
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Vermel electrophoresis - translation to ρωσικά

PHYSICOANALYTICAL TECHNIQUE
Agarose gel; Electrophoresis, agar gel; Agar gel electrophoresis
  • Video showing assembly of the rig and loading/running of the gel.
  • Cutting out agarose gel slices. Protective equipment must be worn when using UV transilluminator.
  • Agarose gel slab in electrophoresis tank with bands of dyes indicating progress of the electrophoresis. The DNA moves towards anode.
  • Loading DNA samples into the wells of an agarose gel using a multi-channel pipette.
  • Gels of plasmid preparations usually show a major band of supercoiled DNA with other fainter bands in the same lane. Note that by convention DNA gel is displayed with smaller DNA fragments nearer to the bottom of the gel. This is because historically DNA gels were run vertically and the smaller DNA fragments move downwards faster.
  • An agarose gel cast in tray, to be used for gel electrophoresis

Vermel electrophoresis      

медицина

электрофорез по Вермелю

agarose gel         

общая лексика

агарозный гель

free-flow electrophoresis         
  • Schematic functionality of Free Flow Electrophoresis
Wikipedia talk:Articles for creation/Free Flow Electrophoresis; Free Flow Electrophoresis

общая лексика

электрофорез в свободном потоке

электрофорез по Гизелиусу

Ορισμός

Cataphoresis
Electric osmore; the transfer of substances in solution through porous membranes under the influence probably of electrolysis, but without themselves being decomposed.

Βικιπαίδεια

Agarose gel electrophoresis

Agarose gel electrophoresis is a method of gel electrophoresis used in biochemistry, molecular biology, genetics, and clinical chemistry to separate a mixed population of macromolecules such as DNA or proteins in a matrix of agarose, one of the two main components of agar. The proteins may be separated by charge and/or size (isoelectric focusing agarose electrophoresis is essentially size independent), and the DNA and RNA fragments by length. Biomolecules are separated by applying an electric field to move the charged molecules through an agarose matrix, and the biomolecules are separated by size in the agarose gel matrix.

Agarose gel is easy to cast, has relatively fewer charged groups, and is particularly suitable for separating DNA of size range most often encountered in laboratories, which accounts for the popularity of its use. The separated DNA may be viewed with stain, most commonly under UV light, and the DNA fragments can be extracted from the gel with relative ease. Most agarose gels used are between 0.7–2% dissolved in a suitable electrophoresis buffer.

Μετάφραση του &#39Vermel electrophoresis&#39 σε Ρωσικά