PSIP1-TBL1X Fusion FISH Probe
The PSIP1-TBL1X Fusion FISH Probe is used to confirm a fusion of the PSIP1 and TBL1X genes. The fusion of the PSIP1 and TBL1X genes has been associated with Pheochromocytoma And Paraganglioma. 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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| PSIP1-TBL1X-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-RERE | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-REOR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-REGO | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-REGR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-REAQ | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-ORRE | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-OROR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-ORGO | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-ORAQ | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GORE | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GOOR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GOGO | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GOGR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GOAQ | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GRRE | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GROR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GRGO | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GRGR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-GRAQ | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-AQRE | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-AQOR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-AQGO | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-AQGR | 20 (40 μL) | 200 μL |
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| PSIP1-TBL1X-20-AQAQ | 20 (40 μL) | 200 μL |
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TBL1X Gene Summary
The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene. [provided by RefSeq, Nov 2008]
Gene Name: Transducin Beta Like 1 X-linked
Chromosome: CHRX: 9431334 -9687780
Locus: Xp22.31-p22.2
PSIP1 Gene Summary
The PC4 And SFRS1 Interacting Protein 1 (PSIP1) gene is located on chr9 :15464064-15511003 at 9p22.3.
Gene Name: PC4 And SFRS1 Interacting Protein 1
Chromosome: CHR9: 15464064 -15511003
Locus: 9p22.3
Gene Diseases
The PSIP1 TBL1X Fusion has been associated with the following diseases:
| Disease Name |
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| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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