Luckau Protocols:Agarose Gel: Difference between revisions

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FYI:
* Migration of gel loading dyes Bromophenol Blue (175bp) and Xylene Cyanol FF (1500bp)
* [[Image:AgaroseGel_2_XCBPB.jpg]]

Revision as of 16:28, 14 January 2011

Agarose Gel Protocol

Tara K. Luckau's Home Page

Conservation Genetics Lab Notebook

Tara's Protocols

Purpose

Agarose gels are used to verify the presence and estimate the size of DNA (both genomic and amplified). When loaded into a gel and subjected to an electric current, DNA fragments migrate to the positive terminal. Small DNA fragments migrate more rapidly than large ones. By running a commercially available ladder of fragments of known size, we can estimate the DNA fragment size in our sample of interest.

To visualize the DNA after electrophoresis, a dye called Gel Red is added during the agarose-making process. The dye binds to the DNA and flouresces when exposed to UV light.

Materials To Be Familiar With

  • Gel Rig, caster tray, combs

Protocol

  1. Make gel using 1x TAE and agarose
    • Use 1% for genomic DNA, 2% for amplified DNA
Gel Rig Size 1x TAE (mL) 1.5% agarose (g) 2% agarose (g) Gel Red (µL) Sample volume (µL) max voltage (V)
small (10cm x 10cm) 50 _ 1 5 4-6 80
medium (x x) 130 _ 2.6 13 24-tooth comb: 6-10 120
36-tooth comb: 3-5
large (20cm x 27cm) 270 _ 5.4 27 24-tooth comb: 6-10 170
36-tooth comb: 3-5

FYI:

  • Migration of gel loading dyes Bromophenol Blue (175bp) and Xylene Cyanol FF (1500bp)