Tips include what to do if insufficient sample migration occurs and why you should look for contamination patterns in graph.
Flick Screen Tape to eliminate bubbles.
Huiyan Jin
NGS Field Application Scientist, North America
If insufficient sample migration occurs, dilute samples to a lower buffer salt concentration.
Kay Wiebrands
Strategic Marketing Manager, SureSeq NGS
Figure 1: Illustrating the differences in quality of input DNA. Blue trace is poor quality FFPE sample with a DIN of 2.3. Green trace is good quality FFPE sample with a DIN score of 5.6. Orange trace is a good quality whole blood DNA sample with a DIN score of 6.5.
Bring all reagents to room temperature.
Kicki Bergefall
FAS Manager - Europe
Protect reagents and working solution from light.
Paul Dougall
Strategic Marketing Manager, CytoSure arrays and NGS
Do not hold assay tubes in hand before measurement.
Pete Gray
Array and NGS Field Application Specialist, Europe
Follow recommended incubation times.
Huiyan Jin
NGS Field Application Scientist, North America
If your reading is too high, dilute samples.
Kay Wiebrands
Strategic Marketing Manager, SureSeq NGS
If you reading is too low, protect from light which diminishes sample signal and check standard tube readings for accuracy.
Kicki Bergefall
FAS Manager - Europe
Carryover contamination may decrease or increase readings, look for contamination patterns in graph.
Paul Dougall
Strategic Marketing Manager, CytoSure arrays and NGS
Check blanking reagent, be sure to use a similar pH and ionic strength as samples solutions to maximise Nanodrop accuracy.
Pete Gray
Array and NGS Field Application Specialist, Europe
