The BioPrime Plus Array CGH Genomic Labeling Systems are a high-performance labeling kits that enable reproducible labeling of genomic DNA samples for array-based Comparative Genomic Hybridization (CGH). Available in both indirect and direct lab

With optimized, proprietary reagents, the Enzo Life Sciences CGH Labeling Kits for oligo arrays produce high quality data using as little as 0.25 µg of genomic DNA, without a need for pre-amplification.

With optimized, proprietary reagents, Enzo’s CYTAG ® SuperCGH Labeling Kits for oligo arrays produce high quality data using as little as 50 ng of genomic DNA, without a need for pre-amplification for precious low input samples. 50 ng DNA samples were labeled with Enzo’s CYTAG ® SuperCGH Labeling Kit for Oligo Arrays or a leading competitor’s kit.

specifically developed and optimized to enzymatically label DNA from blood, cells or frozen tissues. For processing FFPE samples, follow the Agilent Oligonucleotide Array-Based CGH for Genomic DNA Analysis (ULS Labeling for Blood, Cells, Tissues or FFPE) Protocol (publication G4410-90020). FFPE samples are not supported for

Discover our selection of CGH + SNP Microarray Kits and Reagents optimized for laboratory workflow. Our CMA kits and reagents include Labeling kits, DNA purification columns, Human Cot DNA & Hybridization Kits.

This chapter details the methods employed to label, hybridize and detect genomic DNA probes for array-CGH. As a first step, two genomic DNA samples - one test and one reference - are labeled separately using two different fluorescent dyes: generally Cyanine 3 (Cy3; excitation/emission wavelength maxima: 550/568nm) and Cyanine 5 (Cy5; 650/668nm).

The BioPrime® Plus Array CGH Genomic Labeling System uses a mutant form of the Klenow fragment of DNA polymerase I (exo-Klenow) and fluorescently labeled random primers and nucleotides to differentially label genomic DNA samples for analysis using CGH. The kit includes optimized nucleotide mixes

For preparation of Cyanine 3- and Cyanine 5-labeled DNA for hybridization to BAC arrays.The CGH Labeling Kit for BAC Arrays has been optimized to label DNA for dual sample comparative genomic hybridization (CGH) assays on BAC arrays.

Comparative genomic hybridization (CGH) is a molecular cytogenetic method for analysing copy number variations (CNVs) relative to ploidy level in the DNA of a test sample compared to a reference sample, without the need for culturing cells.

Array-based comparative genomic hybridization (aCGH) uses a two-color process to measure DNA copy number changes and copy-neutral Loss of Heterozygosity (LOH) or Uniparental Disomy (UPD)† in an experimental sample relative to a reference (control) sample.