BSC 315 Lecture Notes - Lecture 26: Plasmid, Recombinant Dna, Nucleic Acid Hybridization

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04/04/2016 (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) (cid:1) Dna synthesis in vitro proceeds 5" to 3". Sanger sequencing- employs the biochemistry of dna synthesis. Dna primer complementary to a short sequence in template. Normal dna nucleotides- 2"-deoxy-atp, ctp, gtp, and ttp. Abbreviated as 2"-deoxy-ntp, or dntp ( n = any nucleotide) Lack oxygen on the 2" and 3" carbon (have h instead of oh) Absence of the 3"-oh terminates dna synthesis because next nucleotide cannot be added (dna polymerase requires a 3"-oh to add next base to; cannot join to 3"-h) (cid:1) In sanger sequencing, every newly-made strand ends w/ a ddntp (cid:1) The terminal base can be identified because each ddntp is tagged w/ a different fluorescent dye (cid:1) (cid:1) (cid:1) Dna primer- 18-22 nt long: primer is synthesized by methods of organic chemistry, when mixed w/ the template it matches up via complementary base pairing (dna hybridization)

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