3p gene detection probe (3p25/CEP3)

3p Gene Probe Detection Kit (Fluorescence In Situ Hybridization Method). - 100µL/10 Tests

3p deletion syndrome is a condition that results from a chromosomal change in which a small piece of chromosome 3 is deleted in each cell. The deletion occurs at the end of the short (p) arm of the chromosome. This chromosomal change often leads to intellectual disability, developmental delay, and abnormal physical features. 

Product Introduction
This kit uses Orange fluorescein labeled VHL probe and Green fluorescein labeled CEP3, to combine VHL/CEP3 genes with the target site by in situ hybridization.

Product Main Components

The kit consists of VHL/CEP3 dual color probe

Applicable Instruments
Fluorescence microscopy imaging systems, including fluorescence microscopy and filter sets suitable for DAPI (367/452), Green (495/517), and Orange (547/565).