Molekylærbiologi

Active Motif's ChIP Spike-in Normalization Strategy can be used to normalize ChIP qPCR and ChIP-Seq data to reduce the effects of technical variation and sample processing bias.

CORALL enables streamlined generation of Illumina-compatible libraries within 4.5 hours, featuring seamless integration of Unique Molecular Identifiers (UMIs) and exceptional protocol-inherent strand specificity (>99 %). The fragmentation-free protocol uses Lexogen’s proprietary Strand Displacement Stop and Ligation technologies to deliver complete transcript representation, including start and end sites. All CORALL RNA-Seq V2 Kits and bundles are delivered with Lexogen UDI 12 nt Unique Dual Indexing Sets for Unique Dual Indexing.

The Stool Collection Tubes are designed for stool sample collection and stabilization using a liquid stabilization buffer. The Stool DNA Stabilizer effects inactivation of DNases and prevents degradation of DNA, it preserves the microorganism titre and prelyses bacteria.

Quality tested to ensure optimal performance for detecting biotinylated molecules

DNA-Dependent RNA Polymerase Specific for T3 Promoter Sequences

For ligation of DNA ends.

Buffer Used with T4 DNA Ligase

High-fidelity polymerase useful for mutagenesis reactions, 3'-overhang removal and 5'-overhang fill-in reactions.

T4 PNK catalyzes the transfer of the gamma-phosphate from ATP to the 5'-terminus of polynucleotides or to mononucleotides bearing a 5'-hydroxyl group.

Joins ssRNA or ssDNA onto the 5´-Phosphoryl End of ssRNA or ssDNA

DNA-Dependent RNA Polymerase Specific for T7 Promoter Sequences

Simply the best way to make in vitro mRNA. Combines the benefits of high-yield transcription with those of post-transcriptional capping and tailing all in one kit.

Synthesize up to 150 µg of uridine-containing IVT RNA (U-RNA) from 1 µg of template in two hours. ScriptGuard™ RNase Inhibitor included to protect synthesized RNA from RNase degradation.

Formulated to maximize yields of canonical uridine-containing RNA (U-RNA) from an in vitro transcription (IVT) reaction. Although yield varies with the DNA template and other factors, a standard 30 minute, 20 μl reaction will yield up to 180 μg of RNA from 1 μg of DNA template.