First slide
CytoCell fluorescence in situ hybridisation (FISH) logo.
Chromosome
131821XY
Label
Disease focus
Regulatory status
In vitro diagnostic. This product is intended to be used on amniocytes.

Product summary

  • Technology FISH
  • Application Cytogenetics & rare disease
  • Areas of interest Constitutional
  • Region 13q14.2
    18p11.1-q11.1 (D18Z1)
    21q22.13
    Xp11.1-q11.1 (DXZ1)
    Yp11.1-q11.1 (DYZ3)
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Chromomaps

Overview

Summary

The FAST FISH Prenatal kit allows detection of trisomies 13, 18 and 21 (Patau, Edwards and Down syndromes) and sex chromosome aneuploidies utilising a 2 hour hybridisation protocol.

CytoCell Prenatal kits provide the benefits of:

  • 2 hour hybridisation protocol demonstrating high intensity signals and minimal background.
  • Economical kit formats: 5, 10, 30* or 50* tests.
  • Liquid stable reagents premixed in hybridisation solution and provided with DAPI counterstain.

 

Probe information

Each kit contains the variable probe sets, details of which are listed below:

Probe set 1

  • X centromere Xp11.1-q11.1 (DXZ1) Green
  • Y centromere Yp11.1-q11.1 (DYZ3) Orange
  • 18 centromere 18p11.1-q11.1 (D18Z1) Blue

Probe set 2

  • 13 unique sequence (13q14.2) Green
  • 21 unique sequence (21q22.13) Orange

*Not available for LPF002 and LPF003.

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