PsbA-NC PCR #7 8/14/19

E15 E16 E17 E18 E19 E20 E21 E22 E23 E24 E25 E26

Procedure

PsbA-NC is a plastid primer - Primer info

Samples E15 E16 E17 E18 E19 E20 E21 E22 E23 E24 E25 E26 were used in this PCR (polimerase chain reaction) reaction

Two master mixes were made A Master Mix of water, 2x mytaq mix, 1,788F Primer (concentration: 10 micromolar), 2,218R Primer (concentration: 10 micromolar)

This Master Mix x4.5

Component Volume for 14 reactions(+5% error)
Water 132.3 micoleters
2x mytaq mix 183.75 micoleters
1,788F Primer (concentration: 10 micromolar) 14.7 micoleters
2,218R Primer (concentration: 10 micromolar) 14.7 micoleters
BAS (Borine Serum Albumin) 1 microliter

24 micoleters of this master mix was added to 7 tubes For the 2 negative controls of 25 micoleters water no positive control was available

1 microleter of the DNA samples was added to the coresponding tube

The samples were then placed in the thermocycler set to

Step Temperature Duration cycles
1 94°C 2:00 1
2 63 1:30 1
3 72°C 2:00 1
4 94°C 0:45 36
5 63 1:00 36
6 72°C 1:30 36
7 72°C 2:00 1
8 4°C hold -

these amplified DNA samples were then tested by making a gel

to create the Gel the following steps were taken

1.5g agarose and 75ml 1X TAE buffer were mixed to make a 2% agarose 75ml gel mix the mix was microwaved and swirled until there were no flakes then 1 microliters Gelgreen was added

the mix was left to cool for 5 minutes then poured into the gel mold the gel was left to harden for 30 minutes

once hardened enough Used TAE buffer was poured into the gel box to cover the mold

5 microliter aliquots of DNA samples E15 E16 E17 E18 E19 E20 E21 E22 E23 E24 E25 E26 and the two controls were made 1 microliter of 5x loading dye was added to each

First 3 microliters of the HyperLadder 100bp was added to the first well of the mold then the DNA samples were each added to the wells in the following order

Ladder E15 E16 E17 Negative Control E18 E19 E20 Positive control - E7
Ladder E21 E22 E23 Negative Control E24 E25 E26 Positive control - E7

The voltage was set to 100V and run for 60 minutes

The Gels have not been run yet for this PCR

08-14-19_PsbA-NC_Gel1

08-14-19_PsbA-NC_Gel2

Notes

This PCR was done with the other PCRs from E15-E54 and P1-P16

Written on August 14, 2019