* Offering next-generation sequencing services for ultra low input and single cell samples is a powerful solution for many research applications.* Some of these applications are unable to generate enough sample quantity to meet the minimum input requirements needed for standard library preparation kits, such as stem cell research or working with laser captured materials. * Using RNA from a large group of cells can sometimes mask out the unique gene expression of a minor cellular subtype within a larger population of cells, which could potentially lead to missing important data. * Crb's Ultra Low Input and Single Cell RNA Sequencing service uses Clontech's SMART-Seq® v4 UltraTM Low Input RNA Kit designed for the purposes of sequencing mRNA from low input (10 ng/~1000 cells) or single cell (10 pg) samples.* This allows us to analyze samples not previously sequenceable, and open new doors in the clinical research of studying rare tumour subgroups which may be more prominent in driving cancer growth and lead to attractive therapeutic targets. * Like our standard RNA-Seq services, we can tailor our sequencing services to a wide spectrum of custom needs and provide minimal turnaround time.
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