Intended for use in applications where the presence of RNases may cause a hazard to RNA quality and experiment results, e.g. in RNA isolation, cDNA synthesis, RT-PCR, RT-LAMP, in vitro transcription and translation.

RNase Inhibitor blocks ribonuclease activity of common eukaryotic enzymes such as RNase A, RNase B, RNase C.

Protects your RNA from degradation. Thermally stable RNase Inhibitor ensuring complete RNA protection and integrity - reliable results in downstream applications.

Broad spectrum endopeptidase with a very high specific activity.

Powder and liquid form, bulk available.

Active under a wide range of reaction conditions, including elevated temperatures and SDS presence.

Free of exonucleases, endonucleases, and ribonucleases.

Digestion of proteins, including DNases and RNases, during nucleic acid preparations without compromising isolated DNA or RNA integrity.

High specificity with minimal optimization for developing diagnostic PCR kits. Eliminates amplification of non-specific products and primer-dimers.

Ready-to-use buffered solution of ultrapure deoxynucleoside 5’-triphosphates, supplied as lithium salts solutions.

Freeze-dried form of Reverse Transcriptase - perfect component for developing lyophilized RT-LAMP kits, RT-qPCR, and RT-PCR assays.

TRANSCRIPTME LYO Reverse Transcriptase has increased thermal stability, enabling high yields of full-length cDNA synthesis ready for downstream application.

Starting material: 10 pg – 5 µg of total RNA or 10 pg – 500 ng of mRNA.

Increased thermal stability for high yields of full-length cDNA synthesis ready to use in downstream applications.

High yields of full-length cDNA synthesis.

The perfect component for developing RT-LAMP kits, RT-qPCR, and RT-PCR assays.

Fast, specific one-step Real-Time RT-PCR, giving consistent results across all commonly-used Real-Time PCR platforms. Optimized for multiplex detection. Mu-MLV Reverse Transcriptase, RNase Inhibitor, and ROX solution are included in separate tubes.

Reproducible and efficient first-strand cDNA synthesis and subsequent Real-Time PCR in a single tube. ROX included.

Fast, specific one-step Real-Time RT-PCR, giving consistent results across all commonly-used Real-Time PCR platforms. Optimized for multiplex detection.

Reproducible and efficient first-strand cDNA synthesis and subsequent Real-Time PCR in a single tube.

The addition of PCR Anti-inhibitor to a reaction mixture is an ideal way to eliminate inhibitors in a DNA template isolation.

Carefully composed mixture of alkaline proteins, which counteracts substances inhibiting the PCR reaction.

Additional purification technology results in significantly increased solubility (2.5 fold), increased specific activity, and remarkable purity with DNA content ≤0.1 pg/mg.

Developed for most demanding applications like isolation, purification and sequencing of RNA and DNA.

High specific activity towards double-stranded DNA leaving single-stranded DNA or RNA undamaged in standard conditions.

Extremely useful for rapid and RNA-safe degradation of genomic DNA, where the absence of ribonucleases is critical to maintaining the integrity of RNA.