Microarray & NGS: Sample Submission
Please, follow the procedures below for Sample Submission for labeling and/or hybridization.
The Facility is accessible to any academic investigators from any institution as well as clients from industry. Prior to sending samples, investigators are encouraged to contact the Facility to discuss the required analysis.
The contact information can be found at the bottom of this page.
- For first time users, complete and submit a Customer Information Form that you can download in the following formats
Microsoft WordAdobe Reader - Contact Dr. Sridar Chittur to discuss the specifics of your project.
- After confirmation of project feasibility by e-mail, follow the RNA Quality Assurance Guidelines.
- Complete and submit the RNA submission sheet in the preferred format
Microsoft WordAdobe Reader - Complete and submit the DNA submission sheet in the preferred format
Microsoft WordAdobe Reader
The Adobe Reader software can be downloaded from the Adobe web site
Get Adobe Reader |
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Shipping Instructions
Each sample should be provided in a single 1.5 mL microfuge tube with the initials of the Principle Investigator and a sample number written on the top.
- Purified RNA
RNA in water should be shipped on enough dry ice to cover the tubes entirely and with enough excess ice to allow for sublimation during shipping. RNA in ethanol should be well-sealed (snap cap with parafilm or screw cap) and can be shipped using gel ice packs or on dry ice. - Purified DNA
Gel ice packs can be used for shipping. - Tissue samples
Samples treated in RNAlater (Qiagen) can be shipped at room temperature. Otherwise, tissues should be collected with consideration given to the effects of RNAses – i.e. isolation or dissection should be done swiftly with RNAse-free instruments and collection tubes, then flash-frozen to -80°C. Samples thus collected can then be shipped to us on dry ice. - Cell pellets
Cell pellets (washed with PBS) can be flash frozen to -80°C and shipped on dry ice, or the pelleted cells can be resuspended in Trizol (2 mL), then flash frozen and shipped on dry ice.For adherent cells, wash plate/flask with PBS, add Trizol directly to plate, coat the surface. The cells will slough off after 2 minutes. Pipette cell in Trizol to RNAse free tube, freeze and ship on dry ice.
Contact Information
Laboratory
Marcy Kuentzel, M.S.
(518) 591-7219
Andrew Hayden, B.S.
(518) 591-7219