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.
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.
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.
Equimolar A/C/G/T at 25 mM each simplifies setup and improves run‑to‑run consistency. Ideal for routine and high‑throughput PCR, library construction, and automated pipelines requiring reproducibility.
High‑Purity dUTP suitable for incorporation by many DNA polymerases. Pair with UNG/UDG to minimize carryover contamination in PCR/qPCR. Also useful for labeling and nick translation workflows.
High‑sensitivity reverse transcriptase designed for highly specific, low‑copy detection and structured RNAs. Excels in standard RT, RT‑qPCR, RNA analysis by primer extension, and RACE with clean backgrounds and consistent yields.
HPLC‑purified nucleotides supplied individually at 100 mM for A/C/G/T. Mix and match for optimal performance and balanced incorporation in PCR, qPCR, RT‑PCR, and cloning workflows across instruments.
Antibody-based Hot-Start Taq DNA Polymerase ensures exceptional specificity and yield in demanding PCR applications. Inactive during setup and rapidly activated by heat, it minimizes primer-dimer formation and nonspecific amplification, enabling clean, reproducible results across diverse templates up to 5 kb.
Engineered M‑MuLV RT with reduced RNase H activity and increased thermostability supports reverse transcription up to 55 °C. Capable of high-yield, full-length cDNA synthesis and suitable for RNA‑seq library prep workflows with reliable performance on structurally complex RNA.