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...

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

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

Full-length cDNA amplification selecting on the 5′ cap, giving high specificity for complete transcripts. Preserves both short and long molecules, ...

Full-length cDNA amplification selecting on the 5′ cap, giving high specificity for complete transcripts. Preserves both short and long molecules, ...

Full-length cDNA amplification selecting on the 5′ cap, giving high specificity for complete transcripts. Preserves both short and long molecules, ...

High-purity RNA extraction across a broad range of sample types including cell culture, animal and plant tissue, and fluid samples.For research use...

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...

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...

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

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...

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...

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...

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...

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...

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...

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