DIYbio:Notebook/Keiki Gels

Gel electrophoresis is used to separate DNA or RNA molecules by size. For this experiment, the gel is inside a plastic drinking straw.

Since this is a DIYbio experiment, I emphasize that all of the materials came from regular shops, including Radioshack and an Asian grocery store in Sacramento, CA. This experiment is designed to create a faster and smaller alternative to traditional gel electrophoresis.

At this point, these instructions are for imaging food coloring - take these instructions and figure out how to do DNA, RNA, proteins, and genome fingerprinting.

Better ideas? Edit this page or email: tito at diybio dot org

General Procedure

1. Cast a gel in a straw
2. Load sample
3. Place straw in gel box with running buffer
4. Run the gel

Casting Gels

Making Gel:

1. Measure 1/2 cup of water into a microwaveable glass cup
2. Add 1 tbsp of agar powder into the cup. Stir.
3. Microwave for 2 minutes. (Caution, the glass cup will most likely be too hot to hold. The water will be clear when the agar is fully dissolved - not cloudy If the agar remains undissolved, microwave for another minute, or more.)

How to get the gel into the straws:

1. Cut clear drinking straws to 3 inch sections - each section will hold one sample
2. Lay the straws at the bottom of a small bowl.
3. When the cup of agar is cool enough to pick up, pour the gel into the small bowl.
4. Put a heavy piece of plastic across the top of the straws so that they don't float to the top of the gel. At this point, check that the straws look like they are full of gel and don't have any air bubbles.
5. Wait for the gel to harden, pull your straws out of the gel.

Buffer

1. Measure 1 cup of warm water into a glass cup
2. Add a pinch of salt
3. Stir and microwave the water until the salt dissolves

Loading your sample

1. At this point, your straws are filled with gel.
2. I used a small knife to poke a hole in the straw about 1/2" from one end of the straw. This created a little pocket in the gel, which is where I added a drop of food coloring. (I used 4 straws, 1 for each of the dyes Green, Red, Blue, Yellow)
3. Place the straws in parallel at the bottom of your gel electrophoresis box (or a tupperware container or bowl should be fine). The dye ends should all be facing one direction.
4. Put a heavy piece of plastic across the the top of the straws so they won't float when you add buffer

Connect your power supply

Keiki gels in gel box

#Connect 4 9v batteries in series. I used 4 because that's how many came in the pack from RadioShack ($10)

1. Connect an alligator wire to the positive terminal, and another alligator wire to the negative terminal.
2. Place the alligator wire connected to the positive (+) terminal in the buffer on the side of the straws with NO dye
3. Place the negative (-) terminal at the end with the dye

Run the gel

1. Add your buffer. It should cover the straws completely, as well as the alligator clips.
2. The negative (-) alligator clip immersed in buffer will begin to have bubbles form on its surface.
3. Wait about an hour, depending on how strong your power supply is. You can watch your food coloring separate into its raw colors during this time.
4. Take your straws out of the gel chamber - all the colors should be separated

Blue: becomes blue + red Green: becomes blue + yellow Yellow: yellow, but disappears quickly Red: red

See also

• Agarose gel loading dye

External links

• Wikipedia entry on agarose gel electrophoresis
• Utah gel box [1]
• Original post on TitoJankowski.com: http://titojankowski.com/?p=152