Online Purchasing Account You are logged on as Guest. LoginRegister a New AccountShopping cart (Empty)
United States 

Cytogenetics





Optimized Solutions for Cytogenetics

Delivering superior results for better understanding of genetic disorders, cancers, and other diseases associated with chromosomal abnormalities

Cytogenetics is the study of chromosomal structure which is relied on to detect human developmental abnormalities at various phases including fetal and early childhood development all the way into adulthood. During fetal development, these include syndromes caused by missing or extra chromosomes (aneuploidies), as well as those caused by structural abnormalities in a chromosome such as unbalanced translocations and inversions. Cytogenetic microarray testing can be utilized during pregnancy to aid physicians in determining whether a fetus or newborn has chromosomal anomalies or developmental delays.

Fluorescence in-situ hybridization (FISH) is a type of molecular cytogenetic testing that is used to assess constitutional and acquired chromosomal aberrations by detecting the presence or absence (also referred to as copy number changes), and relative positioning of specific genes by fluorescence microscopy. It can be applied to metaphase chromosome preparations as well as interphase cell nuclei and methodologies can be modified by clinical labs. Microarray comparative genomic hybridization (aCGH) testing is utilized for the detection of genetic imbalances caused by gain or loss of chromosomal material (copy number changes), which may be beyond the detectable range of conventional cytogenetic and FISH techniques.

As pioneers in labeling and detection, we have used our superior labeling technology at Enzo to develop a broad range of molecular tools for the cytogenetics market, including FISH and array CGH solutions. These powerful tools can help provide a greater understanding of the role of chromosomal changes in genetic diseases and cancers.

 

Array CGH

Enable Proven, Consistent Array CGH

Array-based comparative genomic hybridization (aCGH) is a powerful tool for detecting gene copy number gains and losses associated with chromosomal abnormalities. Detecting chromosomal aberrations by aCGH is faster, more robust and provides superior results over other technologies such as FISH and G-banding karyotyping, thus providing a greater understanding of the role of chromosomal changes in genetic diseases and cancers.

Enzo’s proprietary labeling technology generates consistent results that exceed industry standards by increasing accuracy of variant detection, minimizing manual data analysis, increasing efficiency, and reducing overall sample analysis time.

  • Generate the highest quality DLR scores (0.09-0.12) and specific activity of labeling
  • Increase resolution for comprehensive, unbiased analysis of DNA copy number changes
  • Perform total genomic DNA analysis without amplification or complexity reduction





Featured Literature

Brochures
CYTAG® CGH Labeling Kits
 

Make Your Own FISH Probes

Modified Nucleotides & Nick Translation Labeling

Ensure Peak Labeling Performance for FISH Probe Synthesis
Fluorescent dye-dUTPs are recognized as superior to analogous methods that use cumbersome indirect two-step labeling methods. When coupled with the Nick Translation DNA Labeling System, this direct approach provides a simple and efficient method to label DNA for FISH, suitable for a wide range of molecular biology and cytogenetics applications.

  • Eight distinct colors to choose from, spanning the visible light spectrum
  • High signal intensity and good photostability


Make your Own FISH Probes



Labeling DNA probe for FISH analysis.

 

FISH Probes

We do supply FISH Probes thru Axxora, our distribution division.


ZytoLight® SPEC CDKN2A/CEN 3/7/17 Quadruple Color Probe
For the detection of the human CDKN2A gene as well as alpha-satellites of chromosomes 3, 7, and 17 by fluorescence in situ hybridization (FISH).

ZytoLight® SPEC MYC Dual Color Break Apart Probe
For the detection of translocations involving the MYC gene at 8q24.21 by fluorescence in situ hybridization (FISH).

ZytoLight® SPEC MDM2/CEN 12 Dual Color Probe
For the detection of human MDM2 gene and alpha-satellites of chromosome 12 by fluorescence in situ hybridization (FISH).

ZytoLight® SPEC BCL6 Dual Color Break Apart Probe
For the detection of translocations involving the BCL6 gene at 3q27.3 by fluorescence in situ hybridization (FISH).

ZytoLight® SPEC BCL2 Dual Color Break Apart Probe
For the detection of translocations involving the BCL2 gene at 18q21.33 by fluorescence in situ hybridization (FISH).

ZytoLight® SPEC MAML2 Dual Color Break Apart Probe
For the detection of translocations involving the MAML2 gene at 11q21 by fluorescence in situ hybridization (FISH).

Do you need FISH Probes?

Click the button below to get contacted by our team.


 

Recommend this page

 
For Research Use Only. Not for use in diagnostic procedures.
Keep in touch

©2017 Enzo Life Sciences, Inc.,