XL CCND3/IGH DF

Translocation/Dual Fusion Probe

Order Number
D-5147-100-OG
Package Size
100 µl (10 Tests)
Labels
  
Chromosomes
614
Regulatory Status
IVDR

IVDR Certification

This probe is IVDR-certified in compliance with the Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR). For organizational reasons, we currently provide only the IVDD product.

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Intended Purpose

The XL CCND3/IGH DF dual-fusion probe is a qualitative, non-automated test for the detection of IGH::CCND3-rearrangements, t(6;14)(p21.1;q32.3) by fluorescence in situ hybridization (FISH). The product is intended as a diagnostic aid and assists in disease monitoring. The test population consists of patients with confirmed or suspected multiple myeloma (MM). Hybridization is to be performed on methanol/acetic-acid fixed plasma cells.

Product Description

The XL CCND3/IGH DF dual-fusion probe consists of an orange-labeled probe hybridizing to the CCND3 gene and flanking regions at 6p21.1 and a green-labeled probe hybridizing to the IGH gene region at 14q32.3.

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Images

XL CCND3/IGH DF

XL CCND3/IGH DF is hybridized to bone marrow cells, one aberrant cell is shown. A translocation t(6;14)(p21;q32) has occurred generating a signal pattern of two colocalization/fusion signals, one green and one orange signal.

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Expected Patterns

Expected Pattern 1

Normal Cell:
Two green (2G) and two orange (2O) signals.

Expected Pattern 2

Aberrant Cell (typical results):
One green (1G), one orange (1O), and two greenorange colocalization/fusion signals (2GO) resulting from a reciprocal translocation between the respective loci.

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News


IVDR Certification

MetaSystems Probes has received IVDR certification for our initial 26 fluorescence in situ hybridization (FISH) probes from the notified body, BSI. Achieving this milestone was not without its challenges, and we are delighted to have accomplished IVDR certification for this probe set at an early stage.

IVDR Certification