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C11ORF30-CDH23 Fusion FISH Probe

The C11ORF30-CDH23 Fusion FISH Probe is used to confirm a fusion of the C11ORF30 and CDH23 genes. The fusion of the C11ORF30 and CDH23 genes has been associated with Prostate 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
C11ORF30-CDH23-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
C11ORF30-CDH23-20-RERE 20 (40 μL) 200 μL
C11ORF30-CDH23-20-REOR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-REGO 20 (40 μL) 200 μL
C11ORF30-CDH23-20-REGR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-REAQ 20 (40 μL) 200 μL
C11ORF30-CDH23-20-ORRE 20 (40 μL) 200 μL
C11ORF30-CDH23-20-OROR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-ORGO 20 (40 μL) 200 μL
C11ORF30-CDH23-20-ORAQ 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GORE 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GOOR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GOGO 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GOGR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GOAQ 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GRRE 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GROR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GRGO 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GRGR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-GRAQ 20 (40 μL) 200 μL
C11ORF30-CDH23-20-AQRE 20 (40 μL) 200 μL
C11ORF30-CDH23-20-AQOR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-AQGO 20 (40 μL) 200 μL
C11ORF30-CDH23-20-AQGR 20 (40 μL) 200 μL
C11ORF30-CDH23-20-AQAQ 20 (40 μL) 200 μL

CDH23 Gene Summary

This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described. [provided by RefSeq, May 2013]

Gene Name: Cadherin Related 23

Chromosome: CHR10: 73156690 -73575704

Locus: 10q22.1

Gene Diseases

The C11ORF30 CDH23 Fusion has been associated with the following diseases:

Disease Name
Prostate Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.