CYTAG® SuperCGH+SNP Labeling Kit

• Suitable for previously limiting low input samples, including precious biopsy samples
• Validated for blood, amniotic fluid, postnatal, and oncology samples
• Provides excellent dynamic analytical range down to 50 ng
• Shorter workflow has samples ready for hybridization in < 4 hours
• Superior DLR scores (<0.18)
• Ability to perform total genomic DNA analysis without amplification or complexity reduction

Comparative genomic hybridization (aCGH) is a powerful diagnostic tool for detecting DNA copy number gains and losses associated with chromosome abnormalities. aCGH provides an understanding of genetic disorders, cancers and other genomic aberrations.

The CYTAG® SuperCGH+SNP Labeling Kit has been designed to provide higher labeled DNA yield, while still maintaining high specific activity for low-input DNA samples, as low as 100 ng for CGH+SNP and 50 ng for CGH only.