Agarose gel electrophoresis is relatively simple and straight forward to perform. Agarose is a natural linear polysaccharide of galactose and 3,6-anhydrogalactose derived from the agar (an algae) of Gelidium amansii. When dry agarose is dissolved in boiling water, poured into a mold and allowed to cool, gel formation occurs at about 45°C. The fibers soak up water and form a network of double strands held together by hydrogen bonding and hydrophobic interactions. The resulting gel is highly porous with little cross-linking among the linear polymer chains. Pore size in the agarose gel depends on agarose concentration; the higher the concentration, the smaller the pore size. At usual agarose concentrations of 0.4 to 2% (w/v), the pores are large enough to allow even the largest protein molecules to pass unimpeded. Therefore, agarose gel electrophoresis separates charged particles primarily according to charge. Particles with larger charge-to-mass ratio will be propelled through the gel by the electric field at higher velocity. Two repeating units of agarose are shown below. OH OH OH OH CH₂ H H t OH H OH OH On a piece of paper, draw chemical structures (Haworth projections) of galactose and 3,6- anhydrogalactose, the two monomers present in the natural polysaccharide, agarose. Label each with their names and upload your answer.

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Agarose gel electrophoresis is relatively simple and straight forward to perform. Agarose is a
natural linear polysaccharide of galactose and 3,6-anhydrogalactose derived from the agar (an algae)
of Gelidium amansii.
When dry agarose is dissolved in boiling water, poured into a mold and allowed to cool, gel
formation occurs at about 45°C. The fibers soak up water and form a network of double strands
held together by hydrogen bonding and hydrophobic interactions. The resulting gel is highly porous
with little cross-linking among the linear polymer chains.
Pore size in the agarose gel depends on agarose concentration; the higher the concentration, the
smaller the pore size. At usual agarose concentrations of 0.4 to 2% (w/v), the pores are large
enough to allow even the largest protein molecules to pass unimpeded. Therefore, agarose gel
electrophoresis separates charged particles primarily according to charge. Particles with larger.
charge-to-mass ratio will be propelled through the gel by the electric field at higher velocity. Two
repeating units of agarose are shown below.
OH
OH
OH
CH₂ H
H
Ĥ
01 4 H
1
ma
OH
OH
OH
On a piece of paper, draw chemical structures (Haworth projections) of galactose and 3,6-
anhydrogalactose, the two monomers present in the natural polysaccharide, agarose. Label each
with their names and upload your answer.
OH
H
Transcribed Image Text:Agarose gel electrophoresis is relatively simple and straight forward to perform. Agarose is a natural linear polysaccharide of galactose and 3,6-anhydrogalactose derived from the agar (an algae) of Gelidium amansii. When dry agarose is dissolved in boiling water, poured into a mold and allowed to cool, gel formation occurs at about 45°C. The fibers soak up water and form a network of double strands held together by hydrogen bonding and hydrophobic interactions. The resulting gel is highly porous with little cross-linking among the linear polymer chains. Pore size in the agarose gel depends on agarose concentration; the higher the concentration, the smaller the pore size. At usual agarose concentrations of 0.4 to 2% (w/v), the pores are large enough to allow even the largest protein molecules to pass unimpeded. Therefore, agarose gel electrophoresis separates charged particles primarily according to charge. Particles with larger. charge-to-mass ratio will be propelled through the gel by the electric field at higher velocity. Two repeating units of agarose are shown below. OH OH OH CH₂ H H Ĥ 01 4 H 1 ma OH OH OH On a piece of paper, draw chemical structures (Haworth projections) of galactose and 3,6- anhydrogalactose, the two monomers present in the natural polysaccharide, agarose. Label each with their names and upload your answer. OH H
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