2 replies to this topic

[anonymous]

I have been trying very hard to transfer cos-1 cells with a construct cloned into pHM6 vector and then detect the expressed protein with anti-HA antibody.But I never detected my protein although pHM6-lacz positive control worked OK. Is that possible that the protein was lost during lysis? What lyzing buffer is good for this purpose? Also, When I did Western detection, non-specific cellular proteins always gave strong signal. How can I eliminate these anoying bands?Your help will be greatly appreciated!Huating

[Filbert]

Hi! Have a nice day.You could try to change another anti-HA antibody and repeat your experiment.

[anonymous]

Thank you very much for the suggestion. Actually, I just got it work by optimizing a few steps. Now, the problem is the detected protein level is very low. Do you have any idea how to improve the transfection efficiency and protein expression level?