We offer a DNA-to-data service: customers provide DNA samples and receive genotypic data. You can now order our services online!
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For DArT assays, 500 - 1000 ng of restriction enzyme grade DNA, resuspended in aqueous solution such as TE at a concentration of 50 - 100 ng/microliter should be submitted.
The preferred format for submission is 94 samples supplied in sealed 96-well microtiter plates, leaving wells G12 and H12 empty. It is critical that you seal the plate very well. We recommend the use of a standard FULLY SKIRTED, V-bottom well 96-well plate (for example Eppendorf Twin-Tec), sealed with strips of 8 caps (for example FLAT caps from Starstedt ref 65.1998.002), applied carefully one by one, wrapped in glad wrap. Although a 3M adhesive film, when properly applied, taking extreme care of sealing the wells one by one on a warm (not cold) plate, may work, we have seen many failures and do not recommend it. Heat-sealable PCR films DO NOT perform unless heat- sealed properly: this is not recommended.
To avoid leaks and cross contamination of samples during shipment, please follow our recommendations about how to ship DNA samples in [download PDF 72 Kb].
Please, e-mail (samples "at" DiversityArrays.com) us the name of the courrier company you are using and the tracking number of your shipment.
As for all genotyping methods, DNA quality has a major effect on DArT data quality. Therefore, DNA quality of the samples is controled upon arrival by incubating 1 µl of DNA in Restriction Enzyme buffer at 37°C for 2 hours and then running the DNA on a 0.8% agarose gel. Good quality DNA gives a high molecular weight band on the gel.
You can find details about our suggested method of DNA extraction [download PDF 79 Kb]. This method proved to work well for many plant species. There is also alternative method developed by one of our collaborators, which should work equally well [download PDF 85 Kb].
Important for international Customers! Please see the special section on Australian quarantine requirements.