Dear Collegues,

I am in a struggle with a lot of probes on Biofouling.

Unfortunatly, I used the MOST interresting probes for SEM. Specimens were fixed and dried by standard procedures, some Others were simply dired by vacuum (wrong but not the bad way). The first results were promising, but I think the DNA is complete damaged by e-minus and subsequent short RangeX-Ray-Damages.

The Samples were spotted with Ag, but the masive e- might have killed the Probe complete.

PLEASE tell me that I am wrong!!