DNA / RNA Extraktions Kits

The innuPREP SE Blood&Eukaryotic Cells UHMW DNA Kit (m) has been designed for manual isolation of ultra-high molecular weight genomic DNA from cultivated eukaryotic cells or PBMCs for applications such as NanoPore or PacBio sequencing.

Lysis Tube W is a 2.0 mL tube with screw cap (red) containing a mixture of ceramic and steel beads (1.4–1.6 mm and 3.5 mm) for efficient disruption of stool, bacteria, fungi and soil, as well as cell cultures and spores, compatible with commonly used homogenizers.

Lysis Tube A is a 2.0 mL tube with a screw cap (colourless) containing optimized ceramic beads (1.4–1.6 mm) for efficient disruption of plant or animal tissue samples, compatible with all commonly used homogenizers for bead-beating.

The innuPREP DNase I Digest Kit is a highly efficient tool for removing DNA from RNA samples. DNA digestion can be conveniently integrated into the RNA isolation process: DNase I is diluted and applied directly onto the spin filter containing the nucleic acids.

The innuMIX qPCR MasterMix SyGreen Sensitive was developed for fast, highly reproducible real-time PCR on the most common qPCR devices for low-ROX and no-ROX. The innuMIX qPCR MasterMix SyGreen uses a proprietary intercalating dye which does not inhibit PCR.

The PME Food DNA Enrichment Tool is based on a new technology: Polymer Mediated Enrichment. Cells and cell-free DNA from liquid samples are captured by a polymer; this complex is collected by centrifugation and the pellet can be used for further analyses.

Lysis Tube J is a 2.0 mL tube with screw cap (blue) containing optimized steel beads (4.7 mm) for efficient disruption of hard samples as wood, seed or rice grain, compatible with all commonly used homogenizers for bead-beating.

Lysis Tube B is a 2.0 mL tube with a screw cap (blue) containing optimized glass (90–150 μm) beads for efficient disruption of bacteria and fungi samples, compatible with all commonly used homogenizers for bead-beating.

The innuDRY qRT-PCR Mix Probe is designed for efficient cDNA synthesis and subsequent probe-based qPCR in a single tube. Very low copy number targets can be detected specifically with high efficiency. The freeze-dried formulation allows storage at +4°C.