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KIAA1522-PEX10 Fusion FISH Probe

The KIAA1522-PEX10 Fusion FISH Probe is used to confirm a fusion of the KIAA1522 and PEX10 genes. The fusion of the KIAA1522 and PEX10 genes has been associated with Liver Hepatocellular 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
KIAA1522-PEX10-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
KIAA1522-PEX10-20-RERE 20 (40 μL) 200 μL
KIAA1522-PEX10-20-REOR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-REGO 20 (40 μL) 200 μL
KIAA1522-PEX10-20-REGR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-REAQ 20 (40 μL) 200 μL
KIAA1522-PEX10-20-ORRE 20 (40 μL) 200 μL
KIAA1522-PEX10-20-OROR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-ORGO 20 (40 μL) 200 μL
KIAA1522-PEX10-20-ORAQ 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GORE 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GOOR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GOGO 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GOGR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GOAQ 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GRRE 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GROR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GRGO 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GRGR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-GRAQ 20 (40 μL) 200 μL
KIAA1522-PEX10-20-AQRE 20 (40 μL) 200 μL
KIAA1522-PEX10-20-AQOR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-AQGO 20 (40 μL) 200 μL
KIAA1522-PEX10-20-AQGR 20 (40 μL) 200 μL
KIAA1522-PEX10-20-AQAQ 20 (40 μL) 200 μL

PEX10 Gene Summary

This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

Gene Name: Peroxisomal Biogenesis Factor 10

Chromosome: CHR1: 2336240 -2344010

Locus: 1p36.32

KIAA1522 Gene Summary

The (KIAA1522) gene is located on chr1 :33207511-33240571 at 1p35.1.

Gene Name:

Chromosome: CHR1: 33207511 -33240571

Locus: 1p35.1

Gene Diseases

The KIAA1522 PEX10 Fusion has been associated with the following diseases:

Disease Name
Liver Hepatocellular Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.