1q21 and 1p32 anomaly detection probe (1q21 and 1p32)
1q21 and 1p32 Gene Anomaly Probe Detection Kit (Fluorescence In-Situ Hybridization Method). - 100µL/10 Tests
The gain/amplification CKS1B gene at chromosome region 1q21 (1q+) is one of the most common genetic aberrations in multiple myeloma (MM). Amplification of CKS1B is frequently associated with the deletion of the CDKN2C gene at chromosome region 1p32 (1p-), which is also associated with inferior outcomes.
Product Introduction
The kit uses orange fluorescein-labeled 1p32(CDKN2C), and green fluorescein-labeled 1q21(CKS1B), and bind 1p32/1q21gene with the target site by in situ hybridization.
Product Main Components
The kit consists of 1q21 orange-red probe
|
Component name |
Specifications |
Quantity |
Main components |
|
1p32/1q21 orange-red probe |
100μL/Tube |
1 |
1p32 Orange probe, 1q21Green 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).