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FlyChip
Functional Genomics for Drosophila
Cambridge Systems Biology Centre, Tennis Court Road, Cambridge, CB2 1QR, UK  [map]
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Full Moon Biosystems QC kit

Overview

After printing, a random sample of microarrays is stained and then scanned so that we can asses the print quality and constancy. These checks include substrate defects, sub-grid and meta-grid positioning on the substrate, checking that all spots have been printed and the spot morphology. The outlined protocol is based on the method recommended by Full Moon Biosystems (http://www.fullmoonbio.com/).

Equipment and Reagents

Procedure (4 slides, per batch)

  1. Add 25 mL QC solution to a reaction tube
  2. Place printed and blocked slides in the reaction tube
  3. Incubate on an orbital shaker for 1 minute at room temperature
  4. Dip slides in 250 mL 0.05% SDS/0.1 x SSC (5 times)
  5. Dip slides in 250 mL 0.1 x SSC (5 times)
  6. Dip slides in 250 mL MilliQ water (5 times)
  7. Transfer to a microscope slide box with lint-free tissue in the base
  8. Centrifuge at 2000 rpm for 2 minutes
  9. Remove any water droplets from the slide using an air duster
  10. Scan using the cy3-channel of a CCD or dual laser scanner

R. Auburn (18-08-2008).