FAM168A-SNX29 Fusion FISH Probe
The FAM168A-SNX29 Fusion FISH Probe is used to confirm a fusion of the FAM168A and SNX29 genes. The fusion of the FAM168A and SNX29 genes has been associated with Glioblastoma Multiforme. 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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| FAM168A-SNX29-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-RERE | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-REOR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-REGO | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-REGR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-OROR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GORE | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GROR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM168A-SNX29-20-AQAQ | 20 (40 μL) | 200 μL |
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FAM168A Gene Summary
The Family With Sequence Similarity 168 Member A (FAM168A) gene is located on chr11 :73117027-73309228 at 11q13.4.
Gene Name: Family With Sequence Similarity 168 Member A
Chromosome: CHR11: 73117027 -73309228
Locus: 11q13.4
SNX29 Gene Summary
The Sorting Nexin 29 (SNX29) gene is located on chr16 :12070601-12668146 at 16p13.13-p13.12.
Gene Name: Sorting Nexin 29
Chromosome: CHR16: 12070601 -12668146
Locus: 16p13.13-p13.12
Gene Diseases
The FAM168A SNX29 Fusion has been associated with the following diseases:
| Disease Name |
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| Glioblastoma Multiforme |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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