Molecular cloning systems based on Gateway® DNA recombination, restriction enzymes or blunt-end ligation.
AccelerRT® 5G Template Switching RT Enzyme Mix (RNase H-) is a novel RT enzyme that was evolved in vitro from MMLV RT. The enzyme possesses RNA- and DNA-dependent polymerase activities but lacks RNase H activity.
In vitro RNA synthesis refers to the synthesis of RNA from a DNA template using a phage DNA-dependent RNA polymerase (e.g. T7, T3 or SP6 RNA polymerase). IVT products include RNA synthesis systems, nuclear extracts, ribonucleotides, cloning vectors and supporting products for transcription, primer extension and gene expression studies.
The AccelerRT® 5G Full Length cDNA Synthesis & Amplification Kit can synthesize cDNA ranging from 1-1000 cells or 10 pg – 100 ng of total RNA and an Oligo(dT)VN Primer as a reverse primer. The full-length cDNA amplification products can be used to analyze gene expression differences, variable splicing, fusion genes and other genetic regulatory information.
GeneCopoeia SuperCut™ Nuclease is a genetically engineered endonuclease derived from Serratia marcescens. The enzyme degrades all forms of DNA and RNA (single-stranded, double-stranded, linear or circular) and is effective over a wide range of conditions.
