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PLEKHA7-USH1C Fusion FISH Probe

The PLEKHA7-USH1C Fusion FISH Probe is used to confirm a fusion of the PLEKHA7 and USH1C genes. The fusion of the PLEKHA7 and USH1C genes has been associated with Esophageal Carcinoma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

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

SKU Test Kits Buffer Dye Color Order Now
PLEKHA7-USH1C-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-RERE 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-REOR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-REGO 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-REGR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-REAQ 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-ORRE 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-OROR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-ORGO 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-ORAQ 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GORE 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GOOR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GOGO 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GOGR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GOAQ 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GRRE 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GROR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GRGO 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GRGR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-GRAQ 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-AQRE 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-AQOR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-AQGO 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-AQGR 20 (40 μL) 200 μL
PLEKHA7-USH1C-20-AQAQ 20 (40 μL) 200 μL

USH1C Gene Summary

This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

Gene Name: USH1 Protein Network Component Harmonin

Chromosome: CHR11: 17515441 -17565963

Locus: 11p15.1

PLEKHA7 Gene Summary

The Pleckstrin Homology Domain Containing A7 (PLEKHA7) gene is located on chr11 :16809206-17035963 at 11p15.2-p15.1.

Gene Name: Pleckstrin Homology Domain Containing A7

Chromosome: CHR11: 16809206 -17035963

Locus: 11p15.2-p15.1

Gene Diseases

The PLEKHA7 USH1C Fusion has been associated with the following diseases:

Disease Name
Esophageal Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.