Home Basic Research Technology Platforms Genomic Analysis Chromosomal Analysis

Chromosomal Analysis

DNA and RNA Labeling

Brighter probes for enhanced nucleic acids visualization

From prenatal genetic testing to cancer screening and detection, the analysis of chromosomal abnormalities is used to identify genetic diseases and diagnose malignant growth.
Fluorescent DNA or RNA probes are powerful tools for chromosomal visualization and high-resolution gene mapping.

BIOARRAY™ Amplification & Labeling Systems

Greater biotin incorporation and brighter signal for routine GeneChip® analysis

BIOARRAY™ Labeling System

BIOARRAY™ Single-round RNA amplification and biotin labeling system provides greater biotin incorporation and improves antisense RNA (aRNA) yield.

DEEPSEE® Probes for Fluorescence In Situ Hybridization (FISH)

Brighter signal with low background

Normal interphase in a cytological specimen shows two gold (CDKN2A), two red (chromosome 3), two green (chromosome 7) and two aqua (chromosome 17) signals after hybridization with DEEPSEE® CDKN2A/CEN3/7/17 Quad probe (ENZ-GEN440).

SEEBRIGHT® Fluorescent Nucleotides

Optimized for high intensity fluorescence probes

Fluorescence emission profiles of available fluorescent labeled dUTPs. The dye-dUTPs are designed to perform especially well in multi-color applications, such as in situ hybridization and microarray analysis.

AMPIVIEW® RNA probes

Visualize the expression and spatial biology of target genes with ease

Complete Product Range

Detection of HER-2 nucleic acid with AMPIVIEW® HER-2 (AS) RNA probes (blue) in breast cancer tissue specimen.