Hello,
We are working with LC 480 and doing 1 step qPCR.
we are working with 10無, if the settings of the PCR was set to 20無 instead of 10無 like we did, is it a problem?
Our problem is that we did the standard curves (with 10無) and measured 3 plates already (with 10無) but forgot to change the setting of the PCR run from 20無 to 10無, and when we changed it with our fourth plate we had a difference of 7 cp values for the target gene and no difference in regard to the reference gene!
Does this difference has to do with the settings of the LightCycler or is it a normal result that has to do with the samples (taking into consideration that the Standard and the Calibrator of the target gene was also increased by 7 cp values)?
Regards...
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1 reply to this topic
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Trof
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Posted 10 April 2011 - 09:16 PM
From what I heard from Roche representative regarding this question, the volume setting only affect the area in which fluorescence is read, if you set 20ul it will make a wider circle to read fluorescence from, and if you lower the volume, the circle is appropriately reduced. So if you set a 20ul and really have only 10, it just reads wider circle than necessary, which may affect a bit the level of the background fluorescence, but no other things.
It's hard to say what caused your gene to jump 7 Cts.
It's hard to say what caused your gene to jump 7 Cts.
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