A selection of reagents and kits for efficient and reproducible RNA extraction and RNA isolation are available, in addition critical reagents for detecting and destroying RNase.
Arrest™ Extraction Buffer is an optimized combination of various chaotropic agents and RNase inhibitors and has a quick 10 minute single step protocol that isolates high quality total RNA from most species and tissues. Compatible with any RNA extraction method, including extractions based on phenol, chloroform and other organic solvents and detergents.
GET™ Total RNA kit isolates total RNA from contaminating DNA, proteins, and nucleases using our GET™ RNA Spin Columns, using Arrest™ Extraction Buffer to extract the RNA.
Tri-Xtract™ is a convenient, ready-to-use reagent designed for the isolation of total RNA that is free from protein and DNA contamination. The isolated RNA is suitable for Northern blots, dot blot hybridization, in-vitro translation, RNase protection assays and poly (A+) selection.
Silica Magnetic Beads are Fe3O4 magnetic beads coated with a silicon dioxide (SiO2) layer. These serve as a simple and efficient tool for RNA purification to capture released RNA. Compatible with Arrest™ Extraction Buffer.
The Boronate resin is designed for the isolation of ribonucleotide and oligonucleotide RNA. The resin consists of boronic acid covalently linked to a polyacrylamide support that offers simple isolation of small molecular weight compounds that have cis-diol groups.
LongLife™ DNase (Deoxyribonuclease) is a ready to use DNase I preparation to remove contaminating DNA and is provided in solution with a co-factor bivalent metal ion. Longlife™ DNase is supplied in 0.5ml volume (10 Units/µl) in a buffer that ensures its full activity and is RNase free.
RNase Removal & Detection
RNaseOUT™ is uniquely formulated to destroy and remove RNases on contact. Simply spray and rinse. RNaseOUT™ is non-toxic and residue free. RNaseOUT™ allows common equipment to be safely and confidently used for all RNA work.
RNase-DETECT™ is a highly reliable and sensitive method to detect RNase contamination, 10µl of test solution is added to our calibrated RNA substrate vial, incubated, and the result viewed after 10 minutes by agarose electrophoresis.