Dear all,
I am working on identification of exosome related protein markers through western blot antibody probing. In my samples, there is an impurity seen at 66KDa which is obtained during the sample acquisition process. When I am screening for the exosomal marker proteins, the impurity is also binding with the antibody and another unwanted constant band is also seen at35KDa during blot imaging. Here I have used Biorad Precision dual color ladder as a protein standard
I am unable to sort this problem. Help me If any one could.