BIO SCI 99 Lecture Notes - Lecture 7: Reverse Transcriptase, Shuttle Vector, Sanger Sequencing

195 views4 pages

Document Summary

*** must transform into bacteria so you have sufficient plasmid to work with - shuttle vector! Answer: b: want plasmid in both, transform bacteria first, eventually will extract plasmid and transform to yeast to get gfp version. Cloning: express proteins in different organisms, want to express hat1 gene, get hat1 copies during pcr reaction, start sequences for restriction enzymes for the dna segments and plasmids, get sticky ends. Genomic library construction cdna library construction cdna: complimentary dna: start with cellular mrna, mrna template is annealed to synthetic oligonucleotide (oligo-dt) primer, reverse transcriptase and dntps yield a complementary dna strand, forming mrna- Value of dna libraries: as source material to clone a gene. Incubate at 23" c for 5h: add mutagen; distribute into similar aliquots, plate out individual aliquots, replica-plate + incubate, take temperature sensitive cdc-mutant yeast; ura3 (requires uracil) - Incubate at 23" c [temp. sensitive - growth @ 23"c but not 36"]

Get access

Grade+20% off
$8 USD/m$10 USD/m
Billed $96 USD annually
Grade+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
40 Verified Answers
Class+
$8 USD/m
Billed $96 USD annually
Class+
Homework Help
Study Guides
Textbook Solutions
Class Notes
Textbook Notes
Booster Class
30 Verified Answers

Related textbook solutions

Related Documents

Related Questions