FAM114A2-FBN2 Fusion FISH Probe
The FAM114A2-FBN2 Fusion FISH Probe is used to confirm a fusion of the FAM114A2 and FBN2 genes. The fusion of the FAM114A2 and FBN2 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| FAM114A2-FBN2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-RERE | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-REOR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-REGO | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-REGR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-OROR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GORE | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GROR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM114A2-FBN2-20-AQAQ | 20 (40 μL) | 200 μL |
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FBN2 Gene Summary
The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly. [provided by RefSeq, Jul 2008]
Gene Name: Fibrillin 2
Chromosome: CHR5: 127593600 -127873735
Locus: 5q23.3
FAM114A2 Gene Summary
The Family With Sequence Similarity 114 Member A2 (FAM114A2) gene is located on chr5 :153371268-153418497 at 5q33.2.
Gene Name: Family With Sequence Similarity 114 Member A2
Chromosome: CHR5: 153371268 -153418497
Locus: 5q33.2
Gene Diseases
The FAM114A2 FBN2 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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