Hi everyone,
I am new to Q-PCR.
Recently, i have been using SYBgreen Q-PCR to check the relative gene expression . For every samples i did it in triplicate, however, i always get a disaggrement or large variations between the results of my triplicate trials including a difference of Ct value and a non-smooth curve in the amplication plot within a sample with triplicate trials.
I was just wondering how i can improve the smoothness of the amplication plot of those triplicate trials of a sample and what tricks you guys are using in order to have a nice Q-PCR result. I am sure that i have pipetted an equal volume of mastermix into each sample in the eppendorf tube and then into the 96 well plate. And i am sure that i have mixed well the solution by pipetting up and down for about 7 times. Yet, i still get a bad result....
Pls kindly give me some suggestions or tips..
THX everyone!!
Disagreement between triplicate results in Q -PCR
Started by MurphysunHKU, Sep 08 2011 07:45 PM
5 replies to this topic
#1
Posted 08 September 2011 - 07:45 PM
#2
Posted 09 September 2011 - 07:23 PM
What volume of sample are you adding to each reaction? And have you calibrated or at least checked the accuracy of your pipettes lately?
#3
Posted 10 September 2011 - 12:27 AM
I added 10 ul for each reaction. does this have the relationship?
Well i have not checked the accuracy, um.. i dun know but i think it's ok
Well i have not checked the accuracy, um.. i dun know but i think it's ok
#4
Posted 10 September 2011 - 06:20 PM
The reason I asked about the sample volume is that sometimes if the volume is too low, and your pipettes aren't brilliant, the variation in amount of template between replicates can be quite significant.
What kinds of differences in Ct are you getting between triplicates?
What kinds of differences in Ct are you getting between triplicates?
#5
Posted 11 September 2011 - 03:45 PM
The Ct Difference I get is about 1 to 2 cycles. Is it too large?
#6
Posted 13 September 2011 - 12:34 AM
MurphysunHKU, on 11 September 2011 - 03:45 PM, said:
The Ct Difference I get is about 1 to 2 cycles. Is it too large?
You say you added 10 ul of sample to the reaction of what final volume? If it is a cDNA in RT mixture, recommended maximum sample volume is 10% of the final volume. So unless you have a 100ul reaction, that's way too much.
Edited by Trof, 13 September 2011 - 03:47 AM.
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