Gel Blotting

Gel blotting is a technique for visualizing a particular subset of macromolecules — proteins, or fragments of DNA or RNA — initially present in a complex mixture. The steps:

• Separate the molecules by electrophoresis. This is done in a gel which allows the molecules to migrate under the influence of the electric field.

  External Link

  Animation of Gel Electrophoresis

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• "Blot" them with a nitrocellulose filter. For unknown reasons, the molecules stick tightly to the filter and will retain their relative positions when flooded with fluid at the next step.
• Bathe the filter with a solution containing a "probe": a molecule that
  • will combine specifically with the target molecules; that is, the one(s) you are looking for
  • carries a mean of visualization, e.g. a radioactive or fluorescent marker.

The diagram illustrates the procedure for detecting DNA fragments containing a particular sequence.

• DNA is extracted from the cell.
• The DNA is partially digested by a restriction endonuclease.
• The resulting DNA fragments are separated by electrophoresis and then denatured to form single-stranded molecules (ssDNA).
• Without altering their positions, the separated bands of ssDNA are transferred to a nitrocellulose filter and exposed to radiolabeled cDNA or RNA.
• If the probe detects complementary DNA sequences, it will bind to them.
• The presence of the probe in a particular band is revealed by autoradiography.

This procedure was developed by E. M. Southern and the finished product is called a "Southern blot".

Links to examples of Southern blots. 1. Screening for the sickle-cell gene 2. Fingerprinting

The same basic procedure can also be used to separate and visualize RNA molecules and protein molecules. As a humorous extension of the term "Southern blot", these have been dubbed "Northern" and "Western" blots respectively.

Type of Blot	Molecules separated by electrophoresis	Probe
Southern	ssDNA	cDNA or RNA
Northern	denatured RNA	RNA or cDNA
Western	Protein	Antibodies

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