Chromosomes 4, 10 detection probe (CEP4/CEP10)

Chromosomes 4, 10 Centromere Probe Probe Detection Kit - 100µL/10 Tests

Chromosome 10, monosomy 10p, also known as 10p partial monosomy, is a rare genetic condition. This condition results from a mutation or error in a person’s DNA or genes. This can cause birth defects such as malformations of the skull and face, a short neck, or heart defects, as well as intellectual disability and growth delays after birth.

Chromosome 4 (q25–q27) contains the gene for EGF, which measures approximately 120 kb. Exon 24 encodes the precursor EGF, while exons 20 and 21 encode the mature EGF.

Product Introduction
The kit uses orange fluorescein-labeled 4q12 and CEP10 orange probe and green fluorescein-labeled CEP10 green probe to bind 4q12/CEP10 probe to the target detection site by in situ hybridization.

Product Main Components

The kit consists of 4q12/CEP10 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).