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1 Southern Blotting Technique (Southern Analysis) (NOTES) There are three blotting techniques routinely used in molecular biology for detection of a specific DNA, RNA and protein sequence. In DNA and RNA samples, sequence of nucleotides is detected, while in protein samples, amino acid sequence is detected through blotting technique. Southern blotting is a method for detection of a specific DNA sequence (nucleotide sequence) in DNA samples. Edwin Southern The Southern Blotting Technique was named after its inventor, Edwin Southern. He was a British biochemist who developed this technique in Edinburgh (Scotland) in the 1970s. Edwin Southern 2 Procedure High molecular-weight DNA strands (large-sized DNA strands) are cut into smaller fragments using Restriction Endonucleases (RE). Then, the RE-digested DNA fragments are subjected to Agarose gel electrophoresis in order to separate them according to size. Steps in Agarose Gel Electrophoresis If some of the DNA fragments are larger than 15 kb, then prior to blotting, the gel may be treated with an acid (such as dilute HCl), which breaks the DNA into smaller pieces, thus allowing more efficient transfer from the gel to nitrocellulose membrane (discussed in the nest steps). The DNA gel is placed into an alkaline solution (NaOH) to denature the double- stranded DNA fragments into single strands. The denaturation in an alkaline environment may improve binding of the negatively charged DNA to a positively charged nitrocellulose membrane (discussion in next steps). It will also help the hybridization of the radioactive probe with single stranded DNA fragments (discussion in next steps). 3 Agarose gel (ready to use) Gel with separated DNA fragments Transfer of Single stranded DNA fragments to nitrocellulose membrane is facilitated using buffer solution or salt solution system, which is as follows: Southern Blotting (1st step) Weight (0.75 kg) Filter paper towel Nitrocellulose membrane Gel Filter paper wick Salt solution or buffer solution 4 A piece of sponge (or filter paper wick) is placed in a tank containing the buffer or salt solution. Later, Agarose gel, carrying single stranded DNA fragments, is put on top of the sponge. A sheet of nitrocellulose membrane (nitrocellulose filter) is placed on top of the gel. To ensure good and even contact between gel and membrane, pressure is applied evenly to the gel by placing a stack of filter paper-towels (absorbent material) and a weight (0.5 to 0.75 kg) on top of the membrane and gel. Buffer solution (or salt solution) is used to prevent drying of the gel and to transfer the DNA fragments from gel to nitrocellulose membrane. Buffer-transfer by capillary action from a region of high water potential to a region of low water potential (usually facilitated by filter paper tissues) is then used to move the DNA from the gel on to the membrane; ion exchange interactions bind the DNA to the nitrocellulose membrane due to the negative charge of the DNA and positive charge of the membrane. Positions of the DNA fragments on the nitrocellulose membrane are identical to their positions in the gel. Southern Blotting Procedure
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