RIDA®Xtract 24 Blood DNA Kit
Reliable, automated nucleic acid extraction from blood samples
The RIDA®Xtract 24 Blood DNA Kit is a semi-automated solution designed to simplify and standardise the extraction of high-quality nucleic acids from blood samples. Used in combination with the RIDA®Xtract 24 System, it enables reliable purification of DNA (and total nucleic acids) from whole blood and buffy coat specimens, supporting consistent performance across routine laboratory workflows.
Built around magnetic bead separation technology, the kit automates key extraction steps including lysis, binding, washing, and elution. This reduces hands-on time and operator variability while delivering reproducible yields suitable for downstream molecular applications such as PCR-based testing. The guided, on-screen workflow allows laboratories to move from sample loading to purified nucleic acids in approximately 75–85 minutes.

The RIDA®Xtract 24 Blood DNA Kit is optimised for use with fresh or frozen mammalian whole blood and buffy coat samples, including specimens collected using common anticoagulants such as EDTA. Each kit includes all essential consumables required to process up to 48 samples, with reagents supplied ready to use and conveniently stored at room temperature, helping laboratories maintain efficient and organised operations.
Designed for use by trained personnel in qualified laboratory environments, the kit delivers dependable, standardised extraction performance when used exclusively with the RIDA®Xtract 24 System. Supported by R-Biopharm’s global technical network, it offers laboratories a reliable solution for routine blood DNA extraction with confidence in both performance and support.
| Ref | Description | Pack Size | Tests |
|---|---|---|---|
| 93031 | RIDA®Xtract 24 Blood DNA Kit | 48 Reagent Cartridges (6 x 8) 48 Reaction Chambers (6 x 8) | 48 Samples |
RIDA®Xtract 24 extraction kits are intended for in-vitro diagnostics use to extract nucleic acids from clinical samples by authorised clinical testing laboratories in Australia and the European Economic Area; and is included on the Australian Register of Therapeutic Goods (ARTG) and compliant with the European IVD Directive 98/79/EC.

