HIGHLIGHTS
- who: Jaskaren Kohli from the Immunostainings Nevi sections were deparaffinised by placing them in xylene two times for , min eachSections were then rehydrated by washing in serial grades of ethanol (100%, %, %, %) for , min each. Sections were then rinsed in dH O , times for , min each. Antigen retrieval was carried out by placing sections in Tris-EDTA buffer (10mM Tris Base, mM EDTA Solution, .05% Tween, pH, .0) and heating in a microwave for , min. Sections were cooled for , min in antigen retrieval buffer and then rinsed three times in TBS +, .025% Triton , for , min each. Sections were . . .

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