20q gene deletion detection probe (20q12/20q13.12)

20q Gene Deletion Probe Detection Kit (Fluorescence In Situ Hybridization Method). - 100µL/10 Tests

Chromosome 20p deletion is a chromosome abnormality that occurs when there is a missing (deleted) copy of genetic material on the short arm (p) of chromosome 20. The severity and the signs and symptoms depend on the size and location of the deletion and which genes are involved.

Extremely small deletions (microdeletions) involving the distal end of chromosome 20p are relatively common and in some cases are passed from parent to child without causing any health problems (called a familial variant). In other cases, a 20p deletion causes signs and symptoms such as developmental delay, growth delay, learning difficulties, distinctive facial features, birth defects, and/or various medical problems.

Product Introduction
This kit uses orange fluorescein labeled 20q12 orange probe and green fluorescein labeled 20q13.1 green probe. 20q12 / 20q13.1 probe can be combined with the target detection site by in situ hybridization.

Product Main Components

The kit consists of 20q12/20q13.1 dual color probe

Applicable Instruments
Fluorescence microscope imaging system, including fluorescence microscope and filter set suitable for DAPI (367/452), green (495/517) and orange (547/565).