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  2. Moving-boundary electrophoresis - Wikipedia

    en.wikipedia.org/.../Moving-boundary_electrophoresis

    Moving-boundary electrophoresis was developed by Arne Tiselius in 1930. [3] Tiselius was awarded the 1948 Nobel Prize in chemistry for his work on the separation of colloids through electrophoresis, the motion of charged particles through a stationary liquid under the influence of an electric field.

  3. Electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Electrophoresis

    Electrophoresis is the motion of charged dispersed particles or dissolved charged molecules relative to a fluid under the influence of a spatially uniform electric field. As a rule, these are zwitterions with a positive or negative net charge. [1] Electrophoresis is used in laboratories to separate macromolecules based on their charges.

  4. Electrophoretic mobility shift assay - Wikipedia

    en.wikipedia.org/wiki/Electrophoretic_mobility...

    An electrophoretic mobility shift assay (EMSA) or mobility shift electrophoresis, also referred as a gel shift assay, gel mobility shift assay, band shift assay, or gel retardation assay, is a common affinity electrophoresis technique used to study protein–DNA or protein–RNA interactions. This procedure can determine if a protein or mixture ...

  5. Pulsed-field gel electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Pulsed-field_gel...

    Pulsed-field gel electrophoresis (PFGE) is a technique used for the separation of large DNA molecules by applying an electric field that periodically changes direction to a gel matrix. [ 1 ] [ 2 ] Unlike standard agarose gel electrophoresis , which can separate DNA fragments of up to 50 kb, PFGE resolves fragments up to 10 Mb. [ 1 ]

  6. Gel electrophoresis of nucleic acids - Wikipedia

    en.wikipedia.org/wiki/Gel_electrophoresis_of...

    Gel electrophoresis of nucleic acids is an analytical technique to separate DNA or RNA fragments by size and reactivity. Nucleic acid molecules are placed on a gel , where an electric field induces the nucleic acids (which are negatively charged due to their sugar- phosphate backbone) to migrate toward the positively charged anode .

  7. Agarose - Wikipedia

    en.wikipedia.org/wiki/Agarose

    Agarose gel electrophoresis is the routine method for resolving DNA in the laboratory. Agarose gels have lower resolving power for DNA than acrylamide gels, but they have greater range of separation, and are therefore usually used for DNA fragments with lengths of 50–20,000 bp ( base pairs ), although resolution of over 6 Mb is possible with ...

  8. Electrokinetic phenomena - Wikipedia

    en.wikipedia.org/wiki/Electrokinetic_phenomena

    electrophoresis, as motion of charged particles under influence of electric field; electro-osmosis, as motion of liquid in porous body under influence of electric field; diffusiophoresis, as motion of particles under influence of a chemical potential gradient;

  9. Category:Electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Category:Electrophoresis

    Electrophoresis is a method of moving charged particles through a medium by using an electric field induced by electrodes. It is also used to separate molecules with different physical characteristics using electrical charges.