The nCounter is a highly robust solution for multiplex gene expression analysis of up to 800 RNA or protein targets that gets you to reproducible results faster.
Propath offers a complete service: from sample prep to data analysis, with robust QA and rapid turnaround.
RNASeq requires complex steps to convert RNA to cDNA, which is then amplified and quantitated as a proxy for the original RNA.
This process introduces variability which may lead to bias, error and an inability to replicate results.
Nanostring simply counts the native RNA – avoiding cDNA errors and amplification bias – which makes the assay highly reproducible, sensitive and time efficient.
Propath offers a complete nCounter gene/protein expression analysis as a turn-key service.
Simply send us your samples and receive publication ready data in as little as two weeks.
We provide a range of data analysis packages, leaving you free to focus on the biology, without waiting months for bioinformatic reports.
We provide an interactive one-on-one review of data with rich visualisations and publication ready figures.
Data analysis packages can be tailored to meet your requirements.
Our Data Analysis service enables you to:
Advanced analysis options include contamination detection, covariate correction, batch correction and multi-omic analyses
Through our partnership with NanoString, we offer a range of advanced analytical options, including the Tumor Inflammation Signature, which quantifies the magnitude of a peripherally suppressed, adaptive immune response in the tumour microenvironment.
nCounter works well with fresh frozen tissue, FFPE, PBMCs and cell lysates.
Ideally we require 100 ng of total RNA (in a volume of 5 µl) for most gene expression panels, although we have seen successful results from lower inputs. If samples are limited, we can offer enrichment procedures to increase concentration.
For FFPE samples the following are general guidelines:
Large resection specimens with high cellularity – 2 sections of 4 to 5 µm
Small biopsies or specimens with low cellularity – 4 to 10 sections of 4 to 5 µm
Yes, this is possible. The number of slides required will vary by the size and the thickness of the section. Generally, 8 slides or more are recommended for submission.
Propath can also successfully run nCounter analysis from archival FFPE blocks.
Yes. Where RNA concentration allows, it is possible to load a higher concentration of RNA than the recommended 20ng/ µL. The amount loaded may be adjusted according to the fragmentation profile of the sample. We can discuss the utility of this approach during the planning phase of your study.
This of course depends on the number of samples and complexity of the study, but for most studies we can return data files within as little as two weeks, plus an additional week for data analysis.
Up to 55 genes can be added to standard off-the-shelf panels.If your genes of interest are not covered by standard panels, Propath can design a custom CodeSet with up to 800 genes of interest.
Yes. There are multiple options to analyse your data, including through OnRamp’s Rosalind cloud platform and NanoString’s nSolver, which is freely available for download.
Alternatively Propath offers a range of basic and advanced analysis packages, which can be tailored to meet your requirements.