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.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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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 |
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Lung Squamous Cell Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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