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SLC25A13-CD2AP Fusion FISH Probe

The SLC25A13-CD2AP Fusion FISH Probe is used to confirm a fusion of the SLC25A13 and CD2AP genes. The fusion of the SLC25A13 and CD2AP genes has been associated with Rectum Adenocarcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.

** This product is for in vitro and research use only. This product is not intended for diagnostic use.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
SLC25A13-CD2AP-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-RERE 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-REOR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-REGO 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-REGR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-REAQ 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-ORRE 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-OROR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-ORGO 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-ORAQ 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GORE 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GOOR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GOGO 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GOGR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GOAQ 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GRRE 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GROR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GRGO 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GRGR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-GRAQ 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-AQRE 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-AQOR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-AQGO 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-AQGR 20 (40 μL) 200 μL
SLC25A13-CD2AP-20-AQAQ 20 (40 μL) 200 μL

SLC25A13 Gene Summary

This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]

Gene Name: Solute Carrier Family 25 Member 13

Chromosome: CHR7: 95749531 -95951459

Locus: 7q21.3

CD2AP Gene Summary

This gene encodes a scaffolding molecule that regulates the actin cytoskeleton. The protein directly interacts with filamentous actin and a variety of cell membrane proteins through multiple actin binding sites, SH3 domains, and a proline-rich region containing binding sites for SH3 domains. The cytoplasmic protein localizes to membrane ruffles, lipid rafts, and the leading edges of cells. It is implicated in dynamic actin remodeling and membrane trafficking that occurs during receptor endocytosis and cytokinesis. Haploinsufficiency of this gene is implicated in susceptibility to glomerular disease. [provided by RefSeq, Jul 2008]

Gene Name: CD2 Associated Protein

Chromosome: CHR6: 47445524 -47594996

Locus: 6p12.3

Gene Diseases

The SLC25A13 CD2AP Fusion has been associated with the following diseases:

Disease Name
Rectum Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.