2. Setup individual reactions in PCR tubes or plates with optical caps or optical tape:
20 μL Master Mix 1 μL DNA (~ 50 ng genomic DNA)
Machine Setup 1. If the machine status reads "Idle" but a user still has not remove their samples then "Save" the current file to preserve the users data before shutting down. 2. Shut down both the machine and the computer. Turn on the detector first then boot the computer. 3. Launch SDS v1.9 software (don't use v1.7). 4. Create a new template: Dye Layer = SybrGreen Sample Type = Sample type setup. Choose SYBRG for UNKN, NTC. Deselect quencher. Select wells with samples. Set sample type to UNKN (or NTC). 5. Program thermocycle conditions 95oC 5' Hold (Stage I) 95oC 15", 60oC 30", 72oC 30" (x40) (Stage II - this stage is emperic) 60oC 15" Hold (Stage III) 95oC 15" Hold (Stage IV)
Select Stage IV and set ramp time to maximum (19:59).
Select "Show Data Collection..."
Select and delete the documents for stage III and IV.
Select: Set 7700 exposure time for plates 25 (caps), or 10 (film). Reference = Rox (unless no reference is used)
7. Save the template to the "Fero Lab" folder. 8. Place plate in sample block, close lid and shut door. Select "RUN".
Saving and processing data 9. When the machine has finished cycling the status will read, "Idle". Save the file again before quitting. 10. To save dissociation curves: select File > Export... > Multicomponent...