Agarose Gel Electrophoresis Purposes n To understand the

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Agarose Gel Electrophoresis

Agarose Gel Electrophoresis

Purposes n To understand the principle of Gel electrophoresis n To become familiar with

Purposes n To understand the principle of Gel electrophoresis n To become familiar with the part of the electrophoresis setup

What is Electrophoresis? Electrophoresis is a laboratory technique for separating molecules based on their

What is Electrophoresis? Electrophoresis is a laboratory technique for separating molecules based on their charge and size.

Separation of a Mixture of Charged Molecules Charged molecules are separated based on their

Separation of a Mixture of Charged Molecules Charged molecules are separated based on their electrical charge and size. Positive Molecules Analyze Charge Separation Mixture of Charged Molecules Size Separation Identify Purify Negative Molecules

How Separation Occurs 1 - Electrical Charge: n Many molecules (amino acids, proteins, DNA,

How Separation Occurs 1 - Electrical Charge: n Many molecules (amino acids, proteins, DNA, and RNA) have naturally occurring negative and positive charges on them. n The sum of these charges determines the overall charge. ØMolecules with a negative charge (anions) will be attracted to the positively charged node (anode). ØMolecules with a positive charge (cations) will be attracted to the negatively charged node (cathode).

How Separation Occurs 2 - Molecule Size: • The porous material is made of

How Separation Occurs 2 - Molecule Size: • The porous material is made of microscopic particles suspended in a gel. • The microscopic particles attach to one another forming tunnels that act as a sieve to separate the molecules. • Small molecules can move faster than large molecules. Porous Material Proteins Entering Porous Material Smallest Move Fastest

Gel Electrophoresis Gels can be made from substances such as agarose or polyacrylamide. •

Gel Electrophoresis Gels can be made from substances such as agarose or polyacrylamide. • Agarose – a complex sugar chain from red seaweed. • It is commonly used in foods (ice cream, and jellies) and many biological mediums. • It has a large pore size good for separating large molecules quickly. Red Sea Weed • Polyacrylamide – chain of acrylamide molecules. • It is often used to make plastics and rubber. • It has a small pore size good for separating small molecules. Acrylic Acid

Agarose Gel n A porous material derived from red seaweed n Agarose is highly

Agarose Gel n A porous material derived from red seaweed n Agarose is highly purified to remove impurities and charge n Acts as a sieve for separating molecules. n This solid matrix will allow the separation of 1% agarose fragments by size. n Concentration affects molecules migration n Low conc. = larger pores better resolution of larger DNA fragments n High conc. = smaller pores better resolution of smaller DNA fragments 2% agarose

Fragment Resolution Gel Concentration – Is dependant upon the size of the DNA fragments

Fragment Resolution Gel Concentration – Is dependant upon the size of the DNA fragments to be separated.

 • Agarose at Room Temperature is a 3 -Dimentional solid matrix. • The

• Agarose at Room Temperature is a 3 -Dimentional solid matrix. • The smaller the fragments the further the migration or movement through the matrix. small - Power large +

Purposes for Agarose Gel Electrophoresis • Analysis of molecules size • Separation and extraction

Purposes for Agarose Gel Electrophoresis • Analysis of molecules size • Separation and extraction of molecules • Quantification of molecules

Procedure

Procedure

Components of an Electrophoresis System n Power supply and chamber, a source of power

Components of an Electrophoresis System n Power supply and chamber, a source of power supply n Buffer, a fluid mixture of water and ions n Agarose gel, a porous material that molecules migrates through n Gel casting materials

Cathode Anode + Buffer Dyes Power Supply

Cathode Anode + Buffer Dyes Power Supply

Electrophoresis Buffer n TAE (Tris -acetate-EDTA) and TBE (Tris-borate- EDTA) – p. H buffer

Electrophoresis Buffer n TAE (Tris -acetate-EDTA) and TBE (Tris-borate- EDTA) – p. H buffer n Tris Acetic acid provide ions to support conductivity and maintain p. H n EDTA, prevent brake down of molecules n Concentration affects DNA migration n Use of water will produce no migraton n High buffer conc. could melt the agarose gel

Overview of Agarose Gel Electrophoresis • Gel Preparation • Loading the gel • Running

Overview of Agarose Gel Electrophoresis • Gel Preparation • Loading the gel • Running the gel

Agarose is a linear polymer extracted from seaweed.

Agarose is a linear polymer extracted from seaweed.

Agarose Buffer Solution Combine the agarose powder and buffer solution. Use a flask that

Agarose Buffer Solution Combine the agarose powder and buffer solution. Use a flask that is several times larger than the volume of buffer.

Melting the Agarose is insoluble at room temperature (left). The agarose solution is boiled

Melting the Agarose is insoluble at room temperature (left). The agarose solution is boiled until clear (right). Gently swirl the solution periodically when heating to allow all the grains of agarose to dissolve. ***Be careful when boiling - the agarose solution may become superheated and may boil violently if it has been heated too long in a microwave oven.

Migration of molecules in Agarose Rate of migration of a molecule is inversely proportional

Migration of molecules in Agarose Rate of migration of a molecule is inversely proportional to the log of its molecular weight Distance α 1 / log-MW

3 Log- Molecular Weight Best Fit Line 2 1 Distance (mm)

3 Log- Molecular Weight Best Fit Line 2 1 Distance (mm)