Agarose gel

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Agarose Gel

An agarose gel is a type of gel used in molecular biology for the separation of nucleic acids such as DNA and RNA. The gel is formed by the polymerization of agarose powder in a buffer solution. The resulting gel has a porous structure that allows the movement of molecules through it. The size of the pores can be controlled by varying the concentration of agarose in the gel.

Composition and Preparation[edit | edit source]

Agarose is a polysaccharide that is extracted from seaweed. It is a linear polymer made up of repeating units of galactose and 3,6-anhydrogalactose. When agarose is dissolved in a buffer solution and heated, it forms a gel as it cools. The concentration of agarose in the gel determines the size of the pores in the gel. Higher concentrations of agarose create smaller pores.

Uses in Molecular Biology[edit | edit source]

Agarose gels are primarily used in gel electrophoresis, a technique used to separate DNA, RNA, and proteins based on their size and charge. The molecules to be separated are loaded into wells in the gel, and an electric field is applied. The negatively charged nucleic acids or proteins move towards the positive electrode, with smaller molecules moving faster than larger ones.

Agarose gels are also used in southern blotting, northern blotting, and western blotting, techniques used to detect specific sequences of DNA, RNA, and proteins, respectively.

Advantages and Disadvantages[edit | edit source]

Agarose gels have several advantages over other types of gels. They are easy to prepare, have a broad range of separation, and are non-toxic. However, they have lower resolving power than polyacrylamide gels, and are not suitable for separating very small molecules.

See Also[edit | edit source]


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Contributors: Prab R. Tumpati, MD