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FAF1-PTRH2 Fusion FISH Probe

The FAF1-PTRH2 Fusion FISH Probe is used to confirm a fusion of the FAF1 and PTRH2 genes. The fusion of the FAF1 and PTRH2 genes has been associated with Breast Invasive 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.

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

SKU Test Kits Buffer Dye Color Order Now
FAF1-PTRH2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FAF1-PTRH2-20-RERE 20 (40 μL) 200 μL
FAF1-PTRH2-20-REOR 20 (40 μL) 200 μL
FAF1-PTRH2-20-REGO 20 (40 μL) 200 μL
FAF1-PTRH2-20-REGR 20 (40 μL) 200 μL
FAF1-PTRH2-20-REAQ 20 (40 μL) 200 μL
FAF1-PTRH2-20-ORRE 20 (40 μL) 200 μL
FAF1-PTRH2-20-OROR 20 (40 μL) 200 μL
FAF1-PTRH2-20-ORGO 20 (40 μL) 200 μL
FAF1-PTRH2-20-ORAQ 20 (40 μL) 200 μL
FAF1-PTRH2-20-GORE 20 (40 μL) 200 μL
FAF1-PTRH2-20-GOOR 20 (40 μL) 200 μL
FAF1-PTRH2-20-GOGO 20 (40 μL) 200 μL
FAF1-PTRH2-20-GOGR 20 (40 μL) 200 μL
FAF1-PTRH2-20-GOAQ 20 (40 μL) 200 μL
FAF1-PTRH2-20-GRRE 20 (40 μL) 200 μL
FAF1-PTRH2-20-GROR 20 (40 μL) 200 μL
FAF1-PTRH2-20-GRGO 20 (40 μL) 200 μL
FAF1-PTRH2-20-GRGR 20 (40 μL) 200 μL
FAF1-PTRH2-20-GRAQ 20 (40 μL) 200 μL
FAF1-PTRH2-20-AQRE 20 (40 μL) 200 μL
FAF1-PTRH2-20-AQOR 20 (40 μL) 200 μL
FAF1-PTRH2-20-AQGO 20 (40 μL) 200 μL
FAF1-PTRH2-20-AQGR 20 (40 μL) 200 μL
FAF1-PTRH2-20-AQAQ 20 (40 μL) 200 μL

FAF1 Gene Summary

Interaction of Fas ligand (TNFSF6) with the FAS antigen (TNFRSF6) mediates programmed cell death, also called apoptosis, in a number of organ systems. The protein encoded by this gene binds to FAS antigen and can initiate apoptosis or enhance apoptosis initiated through FAS antigen. Initiation of apoptosis by the protein encoded by this gene requires a ubiquitin-like domain but not the FAS-binding domain. [provided by RefSeq, Jul 2008]

Gene Name: Fas Associated Factor 1

Chromosome: CHR1: 50906934 -51425936

Locus: 1p32.3

PTRH2 Gene Summary

The protein encoded by this gene is a mitochondrial protein with two putative domains, an N-terminal mitochondrial localization sequence, and a UPF0099 domain. In vitro assays suggest that this protein possesses peptidyl-tRNA hydrolase activity, to release the peptidyl moiety from tRNA, thereby preventing the accumulation of dissociated peptidyl-tRNA that could reduce the efficiency of translation. This protein also plays a role regulating cell survival and death. It promotes survival as part of an integrin-signaling pathway for cells attached to the extracellular matrix (ECM), but also promotes apoptosis in cells that have lost their attachment to the ECM, a process called anoikos. After loss of cell attachment to the ECM, this protein is phosphorylated, is released from the mitochondria into the cytosol, and promotes caspase-independent apoptosis through interactions with transcriptional regulators. This gene has been implicated in the development and progression of tumors, and mutations in this gene have been associated with an infantile multisystem neurologic, endocrine, and pancreatic disease (INMEPD) characterized by intellectual disability, postnatal microcephaly, progressive cerebellar atrophy, hearing impairment, polyneuropathy, failure to thrive, and organ fibrosis with exocrine pancreas insufficiency (PMID: 25574476). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]

Gene Name: Peptidyl-tRNA Hydrolase 2

Chromosome: CHR17: 57774666 -57784856

Locus: 17q23.1

Gene Diseases

The FAF1 PTRH2 Fusion has been associated with the following diseases:

Disease Name
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.