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PEX13-VPS24 Fusion FISH Probe

The PEX13-VPS24 Fusion FISH Probe is used to confirm a fusion of the PEX13 and VPS24 genes. The fusion of the PEX13 and VPS24 genes has been associated with Lung Squamous Cell 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
PEX13-VPS24-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
PEX13-VPS24-20-RERE 20 (40 μL) 200 μL
PEX13-VPS24-20-REOR 20 (40 μL) 200 μL
PEX13-VPS24-20-REGO 20 (40 μL) 200 μL
PEX13-VPS24-20-REGR 20 (40 μL) 200 μL
PEX13-VPS24-20-REAQ 20 (40 μL) 200 μL
PEX13-VPS24-20-ORRE 20 (40 μL) 200 μL
PEX13-VPS24-20-OROR 20 (40 μL) 200 μL
PEX13-VPS24-20-ORGO 20 (40 μL) 200 μL
PEX13-VPS24-20-ORAQ 20 (40 μL) 200 μL
PEX13-VPS24-20-GORE 20 (40 μL) 200 μL
PEX13-VPS24-20-GOOR 20 (40 μL) 200 μL
PEX13-VPS24-20-GOGO 20 (40 μL) 200 μL
PEX13-VPS24-20-GOGR 20 (40 μL) 200 μL
PEX13-VPS24-20-GOAQ 20 (40 μL) 200 μL
PEX13-VPS24-20-GRRE 20 (40 μL) 200 μL
PEX13-VPS24-20-GROR 20 (40 μL) 200 μL
PEX13-VPS24-20-GRGO 20 (40 μL) 200 μL
PEX13-VPS24-20-GRGR 20 (40 μL) 200 μL
PEX13-VPS24-20-GRAQ 20 (40 μL) 200 μL
PEX13-VPS24-20-AQRE 20 (40 μL) 200 μL
PEX13-VPS24-20-AQOR 20 (40 μL) 200 μL
PEX13-VPS24-20-AQGO 20 (40 μL) 200 μL
PEX13-VPS24-20-AQGR 20 (40 μL) 200 μL
PEX13-VPS24-20-AQAQ 20 (40 μL) 200 μL

PEX13 Gene Summary

This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008]

Gene Name: Peroxisomal Biogenesis Factor 13

Chromosome: CHR2: 61244811 -61279125

Locus: 2p15

Gene Diseases

The PEX13 VPS24 Fusion has been associated with the following diseases:

Disease Name
Lung Squamous Cell Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.