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Can anyone help me? :confused:

I am trying to purify a protein out of a nuclear extract. I know absolutely nothing about this protein (transcription factor), except which DNA sequence it binds to. I try to follow the purification through a gel shift (EMSA) assay and have heard that you can calculate the dissociation constant (Kd) from gel shifts.

Do anyone know how :hyper:

 

I would be thankful for all your help!

 

/Anna

 

Imagination is more important than knowledge...

Albert Einstein

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