FMN1-KIAA1267 Fusion FISH Probe
The FMN1-KIAA1267 Fusion FISH Probe is used to confirm a fusion of the FMN1 and KIAA1267 genes. The fusion of the FMN1 and KIAA1267 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 |
---|---|---|---|---|
FMN1-KIAA1267-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-RERE | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-REOR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-REGO | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-REGR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-REAQ | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-ORRE | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-OROR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-ORGO | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-ORAQ | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GORE | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GOOR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GOGO | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GOGR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GOAQ | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GRRE | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GROR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GRGO | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GRGR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-GRAQ | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-AQRE | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-AQOR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-AQGO | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-AQGR | 20 (40 μL) | 200 μL | ||
FMN1-KIAA1267-20-AQAQ | 20 (40 μL) | 200 μL |
FMN1 Gene Summary
This gene belongs to the formin homology family and encodes a protein that has a role in the formation of adherens junction and the polymerization of linear actin cables. The homologous gene in mouse is associated with limb deformity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]
Gene Name: Formin 1
Chromosome: CHR15: 33057746 -33360085
Locus: 15q13.3
Gene Diseases
The FMN1 KIAA1267 Fusion has been associated with the following diseases:
Disease Name |
---|
Skin Cutaneous Melanoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
---|