Pyrophosphatase, Inorganic

In IVT, accumulating pyrophosphate (PPi) inhibits T7 and other RNA polymerases. Inorganic pyrophosphatase hydrolyzes PPi to phosphate, preventing product inhibition and sustaining transcription for higher, cleaner mRNA yields at standard reaction conditions.

Maximize IVT yield by removing PPi product inhibition
Improve full‑length purity and reduce truncated RNA
Simple spike‑in; no buffer changes to your mix
Cost‑efficient: more mRNA per run saves template and NTPs

T4 RNA Ligase II

T4 RNA Ligase II ligates 3′‑OH RNA to 5′‑phosphorylated oligos in a duplex context, suppressing adapter‑dimers and artifacts. It enables cleaner small RNA libraries and supports dsRNA nick sealing and RNA circularization across scales.

Duplex‑guided ligation suppresses adapter‑dimers
Cleaner small RNA libraries and profiles
Supports dsRNA nick sealing and circularization
Scales from pilot to high‑throughput workflows

Hot-Start DNA Polymerase, High Fidelity

Proofreading hot‑start polymerase delivering higher fidelity than Taq with robust amplification of mid‑length targets. Produces blunt‑end products for cloning and is well‑suited for NGS library amplification.

Higher fidelity than Taq; Proofreading
Robust amplification of 5–10 kb targets
Produces blunt ends ideal for cloning
Reliable for NGS library amplification

DNase I

RNase‑free DNase I rapidly digests plasmid templates after IVT and removes genomic DNA from RNA preps. Protect RNA integrity and prevent false positives in RT‑qPCR and RNA‑seq with a high‑activity enzyme compatible with common buffers.

Rapid post‑IVT template removal
Clear gDNA for accurate RT‑qPCR and RNA‑seq
High activity across common buffers and kits
RNase‑free: preserves RNA integrity

Proteinase K, lyophilized

Broad‑spectrum serine protease rapidly inactivates RNases/DNases and digests proteins. Stable lyophilizate with PCR‑grade purity supports DNA/RNA extraction and cleanup across varied samples and conditions.

Rapid RNase/DNase inactivation
Efficient protein digestion and cleanup
Stable lyophilizate; PCR‑grade purity
Works across varied samples and buffers

Taq DNA Polymerase Antibody

Monoclonal antibody reversibly inhibits Taq at ambient temperature and releases during initial denaturation. Reduces primer‑dimers and mis‑priming for cleaner, more specific amplification setups.

Thermolabile block enables hot‑start PCR
Reduces primer‑dimers and mis‑priming
Room‑temperature setup convenience
Compatible with standard PCR protocols

Reverse Transcription Recombinase Polymerase Amplification (RT-RPA) Endpoint RNA Detection Kit

Integrates reverse transcription with endpoint RPA for fast RNA detection at low constant temperatures. Lyophilized 2× mix simplifies setup for gel or lateral‑flow analysis in ~10–20 minutes.

RT integrated for RNA targets
Rapid results in ~10–20 minutes
37–42 °C low‑temperature detection
Endpoint readout via gel or lateral flow

Reverse Transcription Recombinase Polymerase Amplification (RT-RPA) Real-Time RNA Detection Kit

Integrates reverse transcription with endpoint RPA for fast RNA detection at low constant temperatures. Lyophilized 2× mix simplifies setup for gel or lateral‑flow analysis in ~10–20 minutes.

RT integrated for RNA targets
Rapid results in ~10–20 minutes
37–42 °C low‑temperature detection
Endpoint readout via gel or lateral flow

Recombinase Polymerase Amplification (RPA) Endpoint Kit

Lyophilized 2× master mix for endpoint detection delivers fast amplification in ~10–20 minutes at low constant temperatures. Streamlined setup suits gel or lateral‑flow readouts and rapid assay development.

Fast results in ~10–20 minutes
37–42 °C low‑temperature amplification
Lyophilized 2× mix simplifies setup
Endpoint detection via gel or lateral flow

Taq DNA Polymerase

Standard 5′→3′ DNA polymerase with low 5′→3′ exonuclease and no proofreading. Adds 3′‑A overhangs for TA cloning. Reliable amplification across typical templates and buffers for everyday PCR and genotyping.

Adds 3′‑A overhangs for TA cloning
Reliable across common buffers and templates
Ideal for routine PCR and genotyping
Low 5′→3′ exonuclease; no proofreading