Team:BYU Provo/Notebook/SmallPhage/Winterexp/Period2/Exp/4.10 T7 phage viability assay 3
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2) Only the -5 titer formed plaques. | 2) Only the -5 titer formed plaques. | ||
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'''V) Conclusions''' | '''V) Conclusions''' |
Latest revision as of 13:29, 9 September 2013
Small Phage March - April Notebook: Experiments
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4.10 T7 Phage Viability Test 3
I) Purpose - Test the viability (concentration if possible) of the T7 (new) and T7+ we got - Become familiar with virus tittering techniques II) Expected outcome - Should see multiple plaques forming on a lawn of E coli (confluent growth) - Plaques should decrease in size as the dilution gets smaller III) Reagent record T7 phage + and T7 new ; E coli BL21; Agar: ×2 prepared by Jordan in 500mL glass bottle; LB: prepared by Jordan in big Erlenmeyer flask; overnight bacteria culture: set up on Tues 4/9 at 12pm IV) Actual procedures / observations 1) Dilution series of bacteriophage and its incubation with E coli
2) Perform spot test
3. Phage plaque size test
4) Check up on phage + bacteria viability in 24 hours. IV) Results 1) Plates Both spot tests for T7+ and T7 (new) formed plaques up to section 6. Sections 7-15 had no plaques. T7 (new) spot tests T7+ spot test 2) Only the -5 titer formed plaques. Titer Test V) Conclusions - T7 (new) is able to grow on E coli BL21. - Plaques decrease in size from sections 0-6 in a 1:10 dilution series. After that, no plaques form - T7+ titer of -5 formed many individual plaques, while -10 and -15 didn’t form any.
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