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XCeloSeq   
Lung Cancer Fusion Kit

®

NGS Library Preparation kit for use with FFPE RNA

Product Details

 Home  >  ATOM-Seq Capture Chemistry  >  RNA Enrichment Workflow > XCeloSeq Lung Cancer Fusion Kit

Use ATOM-Seq to capture and enrich for gene fusions from 15 genes which are frequently involved in chromosomal rearrangements in lung cancer. Amplification targeted by only single primers, each amplifying a conserved fusion partner, ensures both known and unknown fusion events are detected. Suitable for even highly damaged FFPE RNA samples.

Specifications

* Higher input masses will provide better sensitivities. Very poor quality material, RIN < 3 and DV200 < 20% can increase input mass to 300 ng

# 8 Additional primers targeting controls are also included.

Target Genes

Targets fusions across 15 genes most frequently involved in generating fusions in lung cancer

Please contact us to discuss customising this panel.

 

Read about all our customisation options here.

Benefits

Simple, single-day protocols leveraging the inherent simplicity and efficiency of DNA polymerases

Process even the lowest quality RNA by capturing both single- and double-stranded cDNA from highly degraded FFPE RNA samples

Identify all fusions (known and unknown) and exon skipping by using a single targeting primer for each conserved exon

Unique Dual Indexes

Unique Dual Indexes (UDIs) are required to be purchased and are sold separately

Please contact us to discuss additional index options.

Resources

Product insert

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SEQ008 Product Insert

For Research Use Only (RUO).

Not for use in diagnostic procedures. Not intended to be used for treatment of human or animal diseases.

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