FAM109B-RAI14 Fusion FISH Probe
The FAM109B-RAI14 Fusion FISH Probe is used to confirm a fusion of the FAM109B and RAI14 genes. The fusion of the FAM109B and RAI14 genes has been associated with Skin Cutaneous Melanoma. 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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| FAM109B-RAI14-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-RERE | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-REOR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-REGO | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-REGR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-OROR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GORE | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GROR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM109B-RAI14-20-AQAQ | 20 (40 μL) | 200 μL |
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RAI14 Gene Summary
The Retinoic Acid Induced 14 (RAI14) gene is located on chr5 :34656432-34832717 at 5p13.2.
Gene Name: Retinoic Acid Induced 14
Chromosome: CHR5: 34656432 -34832717
Locus: 5p13.2
FAM109B Gene Summary
The Family With Sequence Similarity 109 Member B (FAM109B) gene is located on chr22 :42470254-42475442 at 22q13.2.
Gene Name: Family With Sequence Similarity 109 Member B
Chromosome: CHR22: 42470254 -42475442
Locus: 22q13.2
Gene Diseases
The FAM109B RAI14 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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