Molekylärbiologi

RNase H is an endonuclease that specifically hydrolyzes the phosphodiester bonds of RNA hybridized to DNA.

A 3´ to 5´ exoribonuclease that digests all linear RNAs except lariat or circular RNA structures

Produce High-Specific-Activity RNA Probes or Defined RNA Transcripts. Choose from combination systems with T3/T7 or SP6/T7 RNA polymerases

Endonuclease Specific for Single-Stranded DNA and RNA

Spike-in RNA variant control mix of the long SIRVs with SIRV Isoform Mix E0 and the ERCCs

SLAMseq is a high-sensitivity method for time-resolved measurement of newly synthesized and existing RNA in cultured cells. SLAMseq enables resolution of RNA synthesis and degradation kinetics.

DNA-Dependent RNA Polymerase Specific for SP6 Promoter Sequences

Utilizes silica-membrane spin-column technology for efficient and high-purity RNA extraction. Provides rapid extraction in under 1 hour without the use of hazardous chemical. Utilizes silica-membrane spin-column technology for efficient and high-purity RNA extraction. Provides rapid extraction in under 1 hour without the use of hazardous chemical. Utilizes silica-membrane spin-column technology for efficient and high-purity RNA extraction. Provides rapid extraction in under 1 hour without the use of hazardous chemical. Utilizes silica-membrane spin-column technology for efficient and high-purity RNA extraction. Provides rapid extraction in under 1 hour without the use of hazardous chemical.

Fast and highly efficient extraction of RNA free of genomic DNA contamination. The RNA can be recovered as total RNA or split into two fractions, large RNA (> 150 nt) and small RNA (< 150 nt).

Vacuum-based method. No centrifugation required