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RNAi problem - Gene is knocked down, but not protein

shRNA protein RNA rnai sirna knockdown

5 replies to this topic

#1 Jean Lu

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Posted 29 September 2011 - 04:46 AM

hi!
My lab encounter wired problems in shRNAPosted Image . we have several shRNAs that can knockdown their target genes at the mRNA level well. we measure them by real time PCR and has a 70-90% knock down efficiency. we design the primers of RT-PCR at the conserved region of the gene. However, the protein did not knockdown no matter how many days we testedPosted Image . we examined at day3,day6,day9, and day 15 post infection. we are working on human embryonic stem cells renewal and mesenchymal stem cells differentiation. Could somebody give us input? how to troubleshoot this? we appreciate your kind help and opinions!

Best Wishes,
JeanPosted Image

#2 Ambinlab

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Posted 17 January 2012 - 02:37 PM

Dear All,

After spending more than 3 weeks, I got my cloning working. I got three plasmids with the right sequences which (should) express shRNA against my gene of interest.

I transfected 293s with my plasmids and was able to see the GFP, which was a marker on the vector. SO I am pretty sure that the cells were transfected efficiently.

I harvested them after 48h and 72h, but I could not see any knockdown effect on western blot. :(

Should I try RT PCR? Should I design more shRNAs against the same gene?

Any ideas would be highly appreciated

#3 pcrman

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Posted 18 January 2012 - 08:46 AM

Definitely, you should first detect mRNA level by RT-PCR, if no drop in mRNA, then the shRNA is not working, otherwise, probably the half life of your protein is very long.

#4 SJGradStudent

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Posted 03 February 2012 - 08:16 AM

Hi all,

I have been struggling for quite some time to see knockdown at the protein level. I have used both siRNA and shRNA (lentiparticles) and I can see a dramatic reduction (~80% K/D) in the target gene, but I can never detect the protein knockdown. The lenti system I use also has GFP included in the vector as a transduction control. I have tried multiple antibodies at different dilutions and have used a control/overexpressed samples to make sure I am looking at the correct band. I can see get overexpression, just not K/D.

Any ideas why this would be so?

Thanks,
Jordan

#5 scolix

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Posted 03 February 2012 - 01:06 PM

what is the turnover time for the protein of interest? Sometimes, you need to wait for sometime before you can see a reduction in protein levels.

#6 pcrman

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Posted 04 February 2012 - 09:37 PM

As Scolix said, the transfection duration could be critical for you to see drop in protein level. You can harvest cells between 3-5 days following transfection. Are there any isoforms of your gene? It could be that the siRNA is knocking down one of them, while your antibodies recognize other isoforms.





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