The Mag-Bind® Total RNA 96 Kit provides a novel technology for total RNA isolation. This kit allows the rapid and reliable isolation of high-quality total cellular RNA and viral RNA from a wide variety of cells and tissues. Unlike column-based systems, the binding of nucleic acids to magnetic particles occurs in solution resulting in increased binding kinetics and binding efficiency. Particles are also completely re-suspended during the wash steps of the purification protocol, which improves the removal of contaminants and increases nucleic acid purity. Mag-Bind® Total RNA 96 Kit procedure can be fully automated with most robotic workstations.
Protocols are available for the following automated platforms:
For Research Use Only. Not for use in diagnostic procedures.
FEATURES | SPECIFICATIONS |
---|---|
Downstream Application | PCR, Next Generation Sequencing, qPCR, real-time RT-PCR, microarray, Northern blot, poly-A purification |
Elution Volume | 30-50 µL |
Starting Material | Animal Tissue and Cultured Cells |
Starting Amount | 1 x 106 cells or 10 mg tissue |
Processing Mode | Automated; Manual |
Throughput | Up to 96 |
RNA Binding Technology | Magnetic Beads |
Figure 1. RNA Integrity. Total RNA was extracted from 1×106 cells using the Mag-Bind® Total RNA Kit. The RNA samples were analyzed with RNA tape on Agilent’s TapeStation® 2200.
Figure 2. RNA Yield Comparison. RNA was isolated using the Mag-Bind® Total RNA Kit and a comparable column-based kit from Company Q. Elution volumes for company Q were 50 µL; for Omega were 100 µL, RNA was quantified using Thermo Scientific’s NanoDrop® 2000c
Figure 3. 10 mg mouse liver was isolated with the Mag-Bind Total RNA Kit according to protocol. Total RNA concentration determined by optical density measurements using Thermo Scientific’s NanoDrop® 2000c. Total elution volume was 100 µL
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