FERMT1-FAM18B2 Fusion FISH Probe
The FERMT1-FAM18B2 Fusion FISH Probe is used to confirm a fusion of the FERMT1 and FAM18B2 genes. The fusion of the FERMT1 and FAM18B2 genes has been associated with Breast Invasive Carcinoma. 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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| FERMT1-FAM18B2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-RERE | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-REOR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-REGO | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-REGR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-REAQ | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-ORRE | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-OROR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-ORGO | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-ORAQ | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GORE | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GOOR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GOGO | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GOGR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GOAQ | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GRRE | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GROR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GRGO | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GRGR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-GRAQ | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-AQRE | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-AQOR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-AQGO | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-AQGR | 20 (40 μL) | 200 μL |
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| FERMT1-FAM18B2-20-AQAQ | 20 (40 μL) | 200 μL |
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FERMT1 Gene Summary
This gene encodes a member of the fermitin family, and contains a FERM domain and a pleckstrin homology domain. The encoded protein is involved in integrin signaling and linkage of the actin cytoskeleton to the extracellular matrix. Mutations in this gene have been linked to Kindler syndrome. [provided by RefSeq, Dec 2009]
Gene Name: Fermitin Family Member 1
Chromosome: CHR20: 6055491 -6104191
Locus: 20p12.3
Gene Diseases
The FERMT1 FAM18B2 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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