Hi,
I am working on real time PCR using SYBR Green Chemistry. Recently I designed the primers using a software. The results that I got seemed to be perfect. All the design guidelines that should have been ideally met by a primer were met. But when I tried these primers no amplification occurred. I am surprised to see this and cannot understand the reason for this to happen.
I ensured that the primers had Tm within the range 50-60 degrees and appropriate Ta Opt as well. The values of self dimers and cross dimers were also within limits.
Could you please help me with my query ?
Primers Not working
Started by kate, Feb 23 2009 10:17 PM
3 replies to this topic
#1
Posted 23 February 2009 - 10:17 PM
#2
Posted 24 February 2009 - 05:19 AM
Do the primers work in a regular PCR?
#3
Posted 24 February 2009 - 08:53 AM
have a look at this topic too: http://www.protocol-...?showtopic=6498
#4
Posted 24 February 2009 - 03:41 PM
Hi,
i made PCR reaction & RT-pCR, the result was as this :
PCR reaction DNA (sample) give band at 150 bp
PCR reaction DNA(negative control) give band at 150 bp
But
RT- PCR RNA (sample) give band at 150 bp
RT- PCR RNA (negative control) no band (clear)
** please, what is the Explain of this situation ?
*** this band was primer- dimer or other thing ( as Original band " spesific band" )
thanks for and sorry for elongation
saly4ever@hotmail.com
i made PCR reaction & RT-pCR, the result was as this :
PCR reaction DNA (sample) give band at 150 bp
PCR reaction DNA(negative control) give band at 150 bp
But
RT- PCR RNA (sample) give band at 150 bp
RT- PCR RNA (negative control) no band (clear)
** please, what is the Explain of this situation ?
*** this band was primer- dimer or other thing ( as Original band " spesific band" )
thanks for and sorry for elongation
saly4ever@hotmail.com













