:: Search forums :: Top Users :: Reagent
Position: Discussion forums > Bioscience biotechniques discussion forums > Cell biology and histology methods forum
|
pSuper
Posted by: agne (IP Hidden, New member, 1)
Date: September 12, 2005 08:45AM
I’ve used siRNA to knock-down one gene: it worked fine, I got approx. 80 % knock down of the protein. I want to get a cell line constantly expressing shRNA, so I chose pSuper retro puro with the same sequence of hairpin as siRNA oligos. I did transient transfection to HeLa with a construct I’m not getting any knock down! The sequence inside of pSuper is fine according to sequencing. Transfection of pSuper is satisfactory, but I still expect to see some knock down in individual cells. Does anyone have any ideas where the problem might be?
Re: pSuper
Posted by: 3'-UTR (IP Hidden, Unregistered user, )
Date: September 14, 2005 04:42PM
Be sure to rule out IFN effect on your "successful" siRNA knockdown at very beginning.
Be awared that transient siRNA effect sometimes is difficult to translate into stable shRNA expression due to unknown reasons, could be the cell type-specific DICER activity/amount/efficiency, siRNA molecule # per cell, target sequence, off-target effect......
|
We are moving ... Please post to our new community forums


