Wear gloves and goggles protecting from EtBr and UV light
With an EDP (dilute mode) pick up 9 µl TE and 1 µl vortexed DNA sample. Spot this on a place of scrap parafilm, pull it up and down one time, and make a second 10 fold dilution with 9 more µl TE and 1 µl of the first dilution. Spot 5 µl of these dilution on different parts of an EtBr agarous (in TBE with EtBr same as a gel) plate (label the bottom of the plate), if the concentration of the original DNA sample is suspected to be less than 20 µg/ml, then spot 5 µl of the undiluted sample also. Also spot on the plate 5 µl of at least the 2, 5, 10, 15, and 20 µg/ml DNA standard. Let the liquid soak in and invert the plate on the transilluminator and compare, interpolate, and record the unknown spots for fluorescent intensity to the standard. Use the dilution that gives between 2 and 20 µg/ml reading. Back calculate the amount of DNA by the dilution factor. It is best if the sample spots are coded and some one else reads them.
DPN Assay quantitation
Care of handling perchloric acid and DPN
Stock Volume (µl) H2O 140 DNA 10 3N perchloric acid 150 DPA solution 180Cap the tubes and mix by inversion.
3 N perchloric acid: dilute 49.2 ml perchloric acid up to 200 ml with H2O in a hood.
DPA (diphenylamine) solution: In a hood, add 20 µl paraldehyde to 198 ml of glacial acetic acid in 250 ml Erlenmyer flask. With gloves, carefully weigh out 8 g of DPA and add to the above solution, quickly cover with foil, and shake until dissolved. Store in the dark in a fume hood. This solution is stabe for 6 weeks.