1. Horizontal Gel Electrophoresis for Nucleic Acids Introduction for Restriction Enzyme Digest and Polymerase Chain Reaction Labs

2. How do we visualize DNA?  Agarose Gel Electrophoresis Complete a Gel Electrophoresis simulation at: http://gslc.genetics.utah.edu/units/biotech/gel/

3. Important Characteristics of DNA Structure  Nucleus is the “command center”  Chromosomes  Double-stranded  DNA helix  Encoded information in the form of bases = “genetic code”

4. Important Characteristics of DNA Structure  Genetic code: Guanine Guanine Adenine Adenine Cytosine Cytosine Thymine Thymine  Phosphate-Sugar backbone NOTE NOTE  Phosphate groups are negatively charged  The mass:charge ratio is the same for all sizes of DNA fragments

5. Agarose Gel Electrophoresis  Electrolysis: the splitting of water using electricity current splits water into hydrogen ions (H + ) and hydroxyl ions (OH - ) current splits water into hydrogen ions (H + ) and hydroxyl ions (OH - )  Electrophoresis: a method of separating charged molecules in an electrical field; DNA has an overall negative charge  Used to separate DNA fragments by size

6. Components of an Electrophoresis System  Power supply and chamber, a source of negatively charged particles with a cathode and anode  Buffer, a fluid mixture of water and ions  Agarose gel, a porous material that DNA migrates through  Gel casting materials  DNA ladder, mixture of DNA fragments of known lengths  Loading dye, contains a dense material and allows visualization of DNA migration  DNA Stain, allows visualizations of DNA fragments after electrophoresis

7. Buffer Dyes Power Supply + - Agarose gel Cathode Anode

8. Bio-Rad’s Electrophoresis Equipment Precast Ready Agarose Gel Power Supplies

9. Electrophoresis Buffer  TAE (Tris-acetate-EDTA) and TBE (Tris-borate- EDTA) are the most common buffers for duplex DNA  Establish pH and provide ions to support conductivity  Concentration affects DNA migration Use of water will produce no migraton Use of water will produce no migraton High buffer conc. could melt the agarose gel High buffer conc. could melt the agarose gel  New Sodium Borate (SB) buffer allows gels to be run at higher voltages in less time than traditional buffers

10. Agarose Gel  A porous material derived from red seaweed  Acts as a sieve for separating DNA fragments; smaller fragments travel faster than large fragments Plinko Model Plinko Model  Concentration affects DNA migration Low conc. = larger pores  better resolution of larger DNA fragments Low conc. = larger pores  better resolution of larger DNA fragments High conc. = smaller pores  better resolution of smaller DNA fragments High conc. = smaller pores  better resolution of smaller DNA fragments 1% agarose 2% agarose

11. Loading Dye  DNA samples are loaded into a gel AFTER the tank has been filled with buffer, covering the gel  Contains a dense substance, such as glycerol, to allow the sample to "fall" into the sample wells  Contains one or two tracking dyes, which migrate in the gel and allow monitoring of how far the electrophoresis has proceeded.

12. DNA Staining  Allows DNA visualization after gel electrophoresis  Ethidium Bromide  Bio-Safe DNA stains In gel staining In gel staining

13. Agarose Gel DNA Fragme nts Frequent Misconceptions  Each band on the gel represents a single DNA strand...NOT TRUE.  A single band/position in a lane contains only one type of DNA sequence...NOT ALWAYS TRUE.