Blocking oligonucleotides that suppress capture of globin transcripts during library preparation. In whole blood, globin mRNA can dominate the poly...

Blocking oligonucleotides that suppress capture of globin transcripts during library preparation. In whole blood, globin mRNA can dominate the poly...

Synthetic spike-in transcripts designed with realistic isoform and abundance complexity, used to validate and monitor RNA-Seq experiments and to co...

Synthetic spike-in transcripts designed with realistic isoform and abundance complexity, used to validate and monitor RNA-Seq experiments and to co...

Synthetic spike-in transcripts designed with realistic isoform and abundance complexity, used to validate and monitor RNA-Seq experiments and to co...

Synthetic spike-in transcripts designed with realistic isoform and abundance complexity, used to validate and monitor RNA-Seq experiments and to co...

Synthetic spike-in transcripts designed with realistic isoform and abundance complexity, used to validate and monitor RNA-Seq experiments and to co...

Synthetic spike-in transcripts designed with realistic isoform and abundance complexity, used to validate and monitor RNA-Seq experiments and to co...

Synthetic spike-in transcripts designed with realistic isoform and abundance complexity, used to validate and monitor RNA-Seq experiments and to co...

Counts one fragment per transcript from the 3′ end, so reads map directly to expression level and far less sequencing depth is needed than whole-tr...

Counts one fragment per transcript from the 3′ end, so reads map directly to expression level and far less sequencing depth is needed than whole-tr...

Time-resolved measurement of RNA synthesis and degradation through metabolic labelling, distinguishing newly transcribed RNA from pre-existing pool...

Time-resolved measurement of RNA synthesis and degradation through metabolic labelling, distinguishing newly transcribed RNA from pre-existing pool...

Counts one fragment per transcript from the 3′ end, so reads map directly to expression level and far less sequencing depth is needed than whole-tr...

Time-resolved measurement of RNA synthesis and degradation through metabolic labelling, distinguishing newly transcribed RNA from pre-existing pool...

Time-resolved measurement of RNA synthesis and degradation through metabolic labelling, distinguishing newly transcribed RNA from pre-existing pool...

Time-resolved measurement of RNA synthesis and degradation through metabolic labelling, distinguishing newly transcribed RNA from pre-existing pool...

Lexogen 12 nt unique dual indices, supplied as index plates for multiplexing. Dual indexing on both ends allows index-hopping artefacts to be ident...

Lexogen 12 nt unique dual indices, supplied as index plates for multiplexing. Dual indexing on both ends allows index-hopping artefacts to be ident...

Column-based isolation of functional small RNA, independent of species. Isolates the RNA actually loaded into silencing complexes rather than total...

Library preparation for small RNA species — microRNA, piRNA and other short transcripts — using adapter ligation to the 3′ and 5′ ends of the RNA r...

Library preparation for small RNA species — microRNA, piRNA and other short transcripts — using adapter ligation to the 3′ and 5′ ends of the RNA r...

RNA extraction from FFPE material in a single step, validated as an input workflow for Lexogen's FFPE library preparation kits.For research use onl...

RNA extraction from FFPE material in a single step, validated as an input workflow for Lexogen's FFPE library preparation kits.For research use onl...