I am currently working on aptamer development. My ELONA results showed that the Kd value of aptamer is 40uM.

How to decrease the Kd value of aptamer to nM? is this possible?

What is the suitable/best binding buffer for ELONA? I am using PBS+1.5 mM MgCl2 as a binding buffer. Increasing MgCl2 can give better results?

What is the optimum incubation temperature for aptamer (room temperature or 370C)?

Does aptamer-protein incubation time affect the Kd value?

More Kasturi Selvam's questions See All
Similar questions and discussions