GFRA3-TTC8 Fusion FISH Probe
The GFRA3-TTC8 Fusion FISH Probe is used to confirm a fusion of the GFRA3 and TTC8 genes. The fusion of the GFRA3 and TTC8 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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| GFRA3-TTC8-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-RERE | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-REOR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-REGO | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-REGR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-REAQ | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-ORRE | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-OROR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-ORGO | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-ORAQ | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GORE | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GOOR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GOGO | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GOGR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GOAQ | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GRRE | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GROR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GRGO | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GRGR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-GRAQ | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-AQRE | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-AQOR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-AQGO | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-AQGR | 20 (40 μL) | 200 μL |
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| GFRA3-TTC8-20-AQAQ | 20 (40 μL) | 200 μL |
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GFRA3 Gene Summary
The protein encoded by this gene is a glycosylphosphatidylinositol(GPI)-linked cell surface receptor and a member of the GDNF receptor family. It forms a signaling receptor complex with RET tyrosine kinase receptor and binds the ligand, artemin. [provided by RefSeq, Jul 2008]
Gene Name: GDNF Family Receptor Alpha 3
Chromosome: CHR5: 137588068 -137610253
Locus: 5q31.2
TTC8 Gene Summary
This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
Gene Name: Tetratricopeptide Repeat Domain 8
Chromosome: CHR14: 89290977 -89344335
Locus: 14q31.3
Gene Diseases
The GFRA3 TTC8 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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