Cytocell® FISH Probes
High-quality range of FISH probes for the detection of gene rearrangements related to inherited genetic disease and cancer.
CytoSure™ Molecular Arrays
Reliable detection of copy number changes for research into a range of genetic disorders.
CytoSure™ ISCA Arrays
Designed in collaboration with the International Standards for Cytogenomic Arrays (ISCA) Consortium, to deliver standardised, evidence-based designs to the cytogenetic research community.
CytoSure™ ISCA UPD Array
The groundbreaking CytoSure ISCA UPD array allows reliable detection of both DNA copy number variation (CNV) with whole chromosome uniparental disomy (UPD).
CytoSure™ ISCA +SNP Array
The CytoSure ISCA +SNP array combines long oligo aCGH probes for superior copy number variation (CNV) detection with fully research-validated SNP content for accurate identification of loss of heterozygosity (LOH) and uniparental disomy (UPD).
CytoSure™ Syndrome Plus v2 Array
Accurate and reliable detection of DNA aberrations across the genome.
CytoSure™ Aneuploidy Array
Simplified detection of chromosome imbalances.
CytoSure™ Single Cell Aneuploidy Array
Reliable detection of aneuploidies when working with small amounts of amplified DNA.
CytoSure™ Chromosome X Arrays
High-resolution detection of DNA deletions and amplifications in the X chromosome genes.
CytoSure™ Cancer +SNP Arrays
Reliable detection of copy number changes and loss of heterozygosity on a single array for the haematological malignancies and solid cancers
CytoSure™ Custom Designed aCGH Arrays
Focused custom aCGH arrays designed by the microarray experts.
CytoSure™ Genomic DNA Labelling Kits
Efficient and reproducible labelling of DNA samples for use in aCGH.
CytoSure™ Interpret Software
Effortless translation of oligo aCGH data into meaningful results.
SciGene Automation Instruments
Complete automation of the aCGH workflow — from DNA to Scanner.
CytoSure™ Sample Tracking Spike-ins
Confident sample identity tracking for use with CytoSure ISCA arrays.