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Plasma/Serum Circulating and Exosomal RNA Purification Kit (Slurry Format), 0.25 - 5 ml sample input - CE-marked (for IVD) Add to Cart

Cat#: Dx42800-NB
Quantity: 50 preps
Price: 819 €  
Special
737.10 € - valid until 31 March 2019
Supplier: Norgen
Shipping: RT
User Manual  

• CE-IVD marked in accordance with EU Directive 98/79/EC
• Fits into in vitro diagnostic workflows
• Fast and easy processing using a rapid spin-column format
• Isolate, high quality total RNA
• Versatile plasma and serum input volumes (0.25 ml to 5 ml)
• Concentrate circulating RNA into small elution volumes
• Isolate all sizes of circulating RNA, including microRNA


Norgen’s Plasma/Serum Circulating and Exosomal RNA Purification Kit Dx (Slurry Format) provides a fast, reliable and simple procedure for isolating circulating and exosomal RNA from plasma/serum samples for subsequent in vitro diagnostic use. Purification is based on the use of Norgen’s proprietary resin as the separation matrix, and the kit purifies all sizes of RNA, from large mRNA and ribosomal RNA down to small RNAs.

This kit is designed to be used with any downstream application employing enzymatic amplification or other enzymatic modifications of RNA followed by signal detection or amplification. Any diagnostic results generated using the RNA isolated with Plasma/Serum Circulating and Exosomal RNA Purification Kit Dx (Slurry Format) in conjunction with an in vitro diagnostic assay should be interpreted with regard to other clinical or laboratory findings.

To minimize irregularities in diagnostic results, suitable controls for downstream applications should be used.

Norgen’s Plasma/Serum Circulating and Exosomal RNA Purification Kit Dx (Slurry Format) is intended for use by professional users such as technicians, physicians and biologists experienced and trained in molecular biological techniques including RNA isolation.

Norgen’s Plasma/Serum Circulating and Exosomal RNA Purification Kit Dx (Slurry Format) does not provide a diagnostic result. It is the sole responsibility of the user to use and validate the kit in conjunction with a downstream in vitro diagnostic assay.


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