FLNB-RHBDF1 Fusion FISH Probe
The FLNB-RHBDF1 Fusion FISH Probe is used to confirm a fusion of the FLNB and RHBDF1 genes. The fusion of the FLNB and RHBDF1 genes has been associated with Bladder Urothelial 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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| FLNB-RHBDF1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-RERE | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-REOR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-REGO | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-REGR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-REAQ | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-ORRE | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-OROR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-ORGO | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-ORAQ | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GORE | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GOOR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GOGO | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GOGR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GOAQ | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GRRE | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GROR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GRGO | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GRGR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-GRAQ | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-AQRE | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-AQOR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-AQGO | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-AQGR | 20 (40 μL) | 200 μL |
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| FLNB-RHBDF1-20-AQAQ | 20 (40 μL) | 200 μL |
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FLNB Gene Summary
This gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3; boomerang dysplasia; autosomal dominant Larsen syndrome; and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Nov 2009]
Gene Name: Filamin B
Chromosome: CHR3: 57994126 -58157982
Locus: 3p14.3
RHBDF1 Gene Summary
The Rhomboid 5 Homolog 1 (RHBDF1) gene is located on chr16 :108057-122629 at 16p13.3.
Gene Name: Rhomboid 5 Homolog 1
Chromosome: CHR16: 108057 -122629
Locus: 16p13.3
Gene Diseases
The FLNB RHBDF1 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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