P4HB-FAR1 Fusion FISH Probe
The P4HB-FAR1 Fusion FISH Probe is used to confirm a fusion of the P4HB and FAR1 genes. The fusion of the P4HB and FAR1 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 |
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| P4HB-FAR1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-RERE | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-REOR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-REGO | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-REGR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-REAQ | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-ORRE | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-OROR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-ORGO | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-ORAQ | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GORE | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GOOR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GOGO | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GOGR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GOAQ | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GRRE | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GROR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GRGO | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GRGR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-GRAQ | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-AQRE | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-AQOR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-AQGO | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-AQGR | 20 (40 μL) | 200 μL |
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| P4HB-FAR1-20-AQAQ | 20 (40 μL) | 200 μL |
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P4HB Gene Summary
This gene encodes the beta subunit of prolyl 4-hydroxylase, a highly abundant multifunctional enzyme that belongs to the protein disulfide isomerase family. When present as a tetramer consisting of two alpha and two beta subunits, this enzyme is involved in hydroxylation of prolyl residues in preprocollagen. This enzyme is also a disulfide isomerase containing two thioredoxin domains that catalyze the formation, breakage and rearrangement of disulfide bonds. Other known functions include its ability to act as a chaperone that inhibits aggregation of misfolded proteins in a concentration-dependent manner, its ability to bind thyroid hormone, its role in both the influx and efflux of S-nitrosothiol-bound nitric oxide, and its function as a subunit of the microsomal triglyceride transfer protein complex. [provided by RefSeq, Jul 2008]
Gene Name: Prolyl 4-hydroxylase Subunit Beta
Chromosome: CHR17: 79801033 -79818544
Locus: 17q25.3
FAR1 Gene Summary
The protein encoded by this gene is required for the reduction of fatty acids to fatty alcohols, a process that is required for the synthesis of monoesters and ether lipids. NADPH is required as a cofactor in this reaction, and 16-18 carbon saturated and unsaturated fatty acids are the preferred substrate. This is a peroxisomal membrane protein, and studies suggest that the N-terminus contains a large catalytic domain located on the outside of the peroxisome, while the C-terminus is exposed to the matrix of the peroxisome. Studies indicate that the regulation of this protein is dependent on plasmalogen levels. Mutations in this gene have been associated with individuals affected by severe intellectual disability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity (PMID: 25439727). A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jan 2015]
Gene Name: Fatty Acyl-CoA Reductase 1
Chromosome: CHR11: 13690205 -13753893
Locus: 11p15.3
Gene Diseases
The P4HB FAR1 Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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