KIF26B-FMN2 Fusion FISH Probe
The KIF26B-FMN2 Fusion FISH Probe is used to confirm a fusion of the KIF26B and FMN2 genes. The fusion of the KIF26B and FMN2 genes has been associated with Brain Lower Grade Glioma. 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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| KIF26B-FMN2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-RERE | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-REOR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-REGO | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-REGR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-REAQ | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-ORRE | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-OROR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-ORGO | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-ORAQ | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GORE | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GOOR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GOGO | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GOGR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GOAQ | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GRRE | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GROR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GRGO | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GRGR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-GRAQ | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-AQRE | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-AQOR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-AQGO | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-AQGR | 20 (40 μL) | 200 μL |
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| KIF26B-FMN2-20-AQAQ | 20 (40 μL) | 200 μL |
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KIF26B Gene Summary
The protein encoded by this gene is an intracellular motor protein thought to transport organelles along microtubules. The encoded protein is required for kidney development. Elevated levels of this protein have been found in some breast and colorectal cancers. [provided by RefSeq, Mar 2017]
Gene Name: Kinesin Family Member 26B
Chromosome: CHR1: 245318286 -245866428
Locus: 1q44
FMN2 Gene Summary
This gene is a member of the formin homology protein family. The encoded protein is thought to have essential roles in organization of the actin cytoskeleton and in cell polarity. This protein mediates the formation of an actin mesh that positions the spindle during oogenesis and also regulates the formation of actin filaments in the nucleus. This protein also forms a perinuclear actin/focal-adhesion system that regulates the shape and position of the nucleus during cell migration. Mutations in this gene have been associated with infertility and also with an autosomal recessive form of intellectual disability (MRT47). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jul 2017]
Gene Name: Formin 2
Chromosome: CHR1: 240255184 -240638489
Locus: 1q43
Gene Diseases
The KIF26B FMN2 Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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