Hi everyone!
I'm using glutaraldehyde as a spacer to cross-link a primary amino and an enzyme on plat glass. After the step of immerging the support in 2.5% glutaraldehyde solution, one protocol says to use ethanol to drain off fixative and through it for one hour in frige.
I would like to know if this step is necessary? My enzyme will be added in after this step. So, with or without ethanol cleaning, what is the difference?
Best regards!
Zibin