Macquarie Australia/12 August 2011

From 2011.igem.org

Team PCR --- 12/8/2011

Today, we started the PCR process in order to amplify our T7 promoter, HO1, At, Dr.

Step 1) We diluted the primer stock down to a concentration of 100uM. We did this by taking the weight of the primers and multiplying them by 100 and then adding this amount of water to the stock.

So, for example, if our amount of Oligo = 38.3nM, we add 383ul of water (which gives us a concentration of 100uM)

Step 2) We performed a second dilution (1:10) to produce a concentration of 10uM for each primer.

So, 100uM  10uM

Step 3) A master-mix was made containing:

Reactants Volume Water 41.4ul 5x buffer 16ul 10mM DNTP 1.6ul

Step 4) Mix was spun for a couple of seconds. This master mix as divided up into 4 15ul aliquots [you can take out 3 lots of 15ul and keep the final 15ul in the mastermix tube and use that as a housing].

Sep 5) To these 15ul aliquots, we add into each:

Primers (from steps 1-2) and template Volume Forward 2ul Reverse 2ul Plasmid template [Ho, Dr etc] 1ul

What we end up with is 4 reaction tubes with our plasmid template, the primers in the correct dilution. However, we have not put in the taq polymerase yet.

Step 6) We set up the PCR machine with the following protocol:

Initial denaturation – 94oC for 2 minutes

Denaturation – 94oC for 30 sec Annealing – 60oC for 30 seconds ] 10 cycles in total Extension – 72oC for 2min 30sec

THEN

Denaturation – 94oC for 30 sec Annealing – 52oC for 30 seconds ] 15 cycles in total. Extension – 72oC for 2min 30sec

Final extension – 72oC for 10 min Hold period – 4oC for 2 minutes

We’ve labelled the protocol ‘330’ and it’s the same as last years’ protocol with a few additions. Note that we made a mistake during our 15 cycle stage - it should be at 72oC. Our bad.

Step 7) We conducted our PCR! It took 2 hours and 13 minutes to complete.

Step 8) With our PCR complete, we then set about preparing the Chloramphenicol vector [which is the one we need to submit for any medal] as well as the clean up protocol.

Ch vector prep

Reactants Volume DPN1 1ul Xba1 + Spe1 1ul + 1ul 100x BSA 1ul Template DNA - Ch vector 20ul 10x NEBuffer 4 5ul Water 21.5ul Total 50.5ul

Clean up prep:

Sigma GENELUTE PCR clean up kit has the protocol

Step 9) We set up the nanodrop to determine the quality of our PCR results:

PCR product Concentration T7 1.1ug [23ng/ul] Ho 870ng [17.4ng/ul] Agro 500ng [10.4ng/ul] Dino 1.8ug [36.1ng/ul]

Step 10) Cleaned PCR products were diluted with water [20ul PCR product + 30ul water] and were then double digested using X + S [1ul each] in 5ul of 10x buffer and 1ul of BSA.