Samples are commonly stored in a way that degrades RNA. Scientists are devising new ways to overcome this obstacle for RNA sequencing. RNA is more subject to degradation than DNA, whether chemical, ...

Traditional PCR systems require users to set a specified number of cycles according to the assay and the input amount. As a result, input material must be quantified, and samples of varying inputs ...

Our staff has over 30 years of combined experience with different RNA library prep kits, from high quality samples to FFPE. We provide free consultations to all users before submitting a project to ...

When carrying out conventional PCR workflows users have to specify how many amplification cycles they need according to input quantity and assay type. This rigid structure is particularly difficult ...

SMART-Seq® Total RNA Pico Input with UMIs (ZapR® Mammalian) is designed for efficient preparation of Illumina sequencing libraries from picogram input amounts of total RNA. Proprietary SMART ...

While widely adopted for comprehensive transcriptome profiling, the methods of poly-A selected or ribodepleted RNA-sequencing may have key limitations, including input mass requirements, inefficient ...