I'm having trouble with bacterial contamination of microglial cultures - dissection is done under a hood and all buffers and reagents have been checked for contamination. (Funny thing, the first time it happened, bacteria was found in the antibiotic itself.)
Does anyone have tips to prevent contamination during the dissection? Since I'm dissecting multiple mice at one time, I think the contamination could be coming from the mouse fur or other areas and am not sure of a good method to reduce that.