CGH labeling kit, CYTAG®
Leverantör: ENZO LIFE SCIENCES
Certifikat
Om denna produkt
Comparative genomic hybridisation (CGH) is a powerful diagnostic tool for detecting DNA copy number gains and losses associated with chromosome abnormalities. CGH provides an understanding of genetic disorders, cancers and other genomic aberrations.
- Compatible with CGH and CGH+SNP arrays
- Ability to perform total genomic DNA analysis without amplification or complexity reduction
- Provides excellent dynamic analytical range for challenging and complex, heterogeneous samples
- QC benchmarked and validated using high resolution arrays
- Superior DLR scores (0,09 – 0,12), exceeding industry standards
These kits produce high quality data using as little as 0,25 µg of genomic DNA, without a need for pre-amplification.
Delivery: Supplied with primers/reaction buffer, cyanine 3-dUTP nucleotide mix, cyanine 5-dUTP nucleotide mix, Klenow Exo-DNA polymerase, stop buffer, nuclease-free water, PCR and gel clean-up columns, AluI, 10X cutting buffer, RsaI, 10X cutting buffer.