Maxam and Gilbert Sequencing Method initiate by DNA extraction and denature double strand DNA molecule to single fragments and radiolabel single fragments on 5’ ends using gamma 32P ATP After that cleave single fragments at specific positions using four chemicals reactions to generate breaks in specific nucleotides as follow: Tub- 1 contain dimethyl sulfate to break guanine nucleotide and Tube-2 contain dimethyl sulfate and formic acid to break purine nucleotides and Tube-3 contain hydrazine to break pyrimidine nucleotide and Tube-4 contain hydrazine and sodium chloride to break cytosine nucleotide and incubate four reactions tubes with piperidine to break modified strands and subject reactions side by side in denature polyacrylamide gel electrophoresis to differentiate fragments size according to radiolabels and autoradiography gel on X-ray film to read gel bands from bottom to top, Bands present in cytosine and pyrimidine nucleotides refer to cytosine nucleotide and bands present in pyrimidine nucleotides refer to thymine nucleotide and bands present in guanine and purine nucleotides refer to guanine nucleotide and bands present in purine nucleotides refer to adenine nucleotide (Watch Related Video in #geneticteacher)
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