Charlie Wilkes
Illuminator
- Joined
- Dec 8, 2009
- Messages
- 4,177
Fulcanelli writes:
Oh Charlie...you've just invented this (note all, the absent 'gel control' raised for the very first time by the FOA on the 1st May - that even rhymes).
Here is an article on the web that talks about controls:
http://faculty.unlv.edu/wmojica/PCR_LAB2.htm
Excerpt:
"Since PCR is so sensitive we should always use a positive and negative control. The positive control should be a PCR mix with DNA known to work in amplification. The negative control should be a PCR mix without DNA. The experimental part should be your PCR mix with DNA."
Was this done when they tested the knife? My understanding is that the lab has not provided the data necessary to answer this question.
Oh Charlie...you've just invented this (note all, the absent 'gel control' raised for the very first time by the FOA on the 1st May - that even rhymes).
Here is an article on the web that talks about controls:
http://faculty.unlv.edu/wmojica/PCR_LAB2.htm
Excerpt:
"Since PCR is so sensitive we should always use a positive and negative control. The positive control should be a PCR mix with DNA known to work in amplification. The negative control should be a PCR mix without DNA. The experimental part should be your PCR mix with DNA."
Was this done when they tested the knife? My understanding is that the lab has not provided the data necessary to answer this question.



