PEX1-RAB34 Fusion FISH Probe
The PEX1-RAB34 Fusion FISH Probe is used to confirm a fusion of the PEX1 and RAB34 genes. The fusion of the PEX1 and RAB34 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.
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
PEX1-RAB34-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-RERE | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-REOR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-REGO | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-REGR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-REAQ | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-ORRE | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-OROR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-ORGO | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-ORAQ | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GORE | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GOOR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GOGO | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GOGR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GOAQ | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GRRE | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GROR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GRGO | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GRGR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-GRAQ | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-AQRE | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-AQOR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-AQGO | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-AQGR | 20 (40 μL) | 200 μL | ||
PEX1-RAB34-20-AQAQ | 20 (40 μL) | 200 μL |
PEX1 Gene Summary
This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]
Gene Name: Peroxisomal Biogenesis Factor 1
Chromosome: CHR7: 92116336 -92157845
Locus: 7q21.2
RAB34 Gene Summary
This gene encodes a protein belonging to the RAB family of proteins, which are small GTPases involved in protein transport. This family member is a Golgi-bound member of the secretory pathway that is involved in the repositioning of lysosomes and the activation of macropinocytosis. Alternative splicing of this gene results in multiple transcript variants. An alternatively spliced transcript variant produces the nine-amino acid residue-repeats (NARR) protein, which is a functionally distinct nucleolar protein resulting from a different reading frame. [provided by RefSeq, Dec 2016]
Gene Name: RAB34, Member RAS Oncogene Family
Chromosome: CHR17: 27041298 -27045286
Locus: 17q11.2
Gene Diseases
The PEX1 RAB34 Fusion has been associated with the following diseases:
Disease Name |
---|
Prostate Adenocarcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
---|