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文献和实验Design and Equipment for the Cell Culture Laboratory
). If this is not possible work should be separated by time with all manipulations on clean material being completed prior to manipulations involving the ‘quarantine material’. Different incubators should also be designated. In addition, the work surfaces
temperature for exactly 5 minutes. Using clean forceps remove the microarray and blow dry with dry nitrogen. Insert the slide into the scanner and scan according the manufacturer’s instruction booklet. For Agilent scanner insert the slide
Basic Methods of Culturing Drosophila
. This is particularly important if a problem is evident. Clean the bench top and all equipment that comes into contact with potentially contaminated stocks with 10% bleach, 70% ethanol or soap and water after use. Sharing pounding pads, CO2 pads, fly pushers and sorting
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