PSAP-OFD1 Fusion FISH Probe
The PSAP-OFD1 Fusion FISH Probe is used to confirm a fusion of the PSAP and OFD1 genes. The fusion of the PSAP and OFD1 genes has been associated with Uterine Carcinosarcoma. 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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| PSAP-OFD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-RERE | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-REOR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-REGO | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-REGR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-REAQ | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-ORRE | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-OROR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-ORGO | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GORE | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GOOR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GOGO | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GOGR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GRRE | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GROR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GRGO | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GRGR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-AQRE | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-AQOR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-AQGO | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-AQGR | 20 (40 μL) | 200 μL |
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| PSAP-OFD1-20-AQAQ | 20 (40 μL) | 200 μL |
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PSAP Gene Summary
This gene encodes a highly conserved preproprotein that is proteolytically processed to generate four main cleavage products including saposins A, B, C, and D. Each domain of the precursor protein is approximately 80 amino acid residues long with nearly identical placement of cysteine residues and glycosylation sites. Saposins A-D localize primarily to the lysosomal compartment where they facilitate the catabolism of glycosphingolipids with short oligosaccharide groups. The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities. Mutations in this gene have been associated with Gaucher disease and metachromatic leukodystrophy. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]
Gene Name: Prosaposin
Chromosome: CHR10: 73576054 -73611082
Locus: 10q22.1
OFD1 Gene Summary
This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified; a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome. [provided by RefSeq, Aug 2016]
Gene Name: OFD1, Centriole And Centriolar Satellite Protein
Chromosome: CHRX: 13752831 -13787480
Locus: Xp22.2
Gene Diseases
The PSAP OFD1 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Carcinosarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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