TSPAN9-KRT86 Fusion FISH Probe
The TSPAN9-KRT86 Fusion FISH Probe is used to confirm a fusion of the TSPAN9 and KRT86 genes. The fusion of the TSPAN9 and KRT86 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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| TSPAN9-KRT86-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-RERE | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-REOR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-REGO | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-REGR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-REAQ | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-ORRE | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-OROR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-ORGO | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-ORAQ | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GORE | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GOOR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GOGO | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GOGR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GOAQ | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GRRE | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GROR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GRGO | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GRGR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-GRAQ | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-AQRE | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-AQOR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-AQGO | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-AQGR | 20 (40 μL) | 200 μL |
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| TSPAN9-KRT86-20-AQAQ | 20 (40 μL) | 200 μL |
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KRT86 Gene Summary
This gene encodes a type II keratin protein, which heterodimerizes with type I keratins to form hair and nails. This gene is present in a cluster of related genes and pseudogenes on chromosome 12. Mutations in this gene have been observed in patients with the hair disease monilethrix. [provided by RefSeq, Feb 2016]
Gene Name: Keratin 86
Chromosome: CHR12: 52695648 -52702947
Locus: 12q13.13
TSPAN9 Gene Summary
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. Alternatively spliced transcripts encoding the same protein have been identified. [provided by RefSeq, Nov 2009]
Gene Name: Tetraspanin 9
Chromosome: CHR12: 3186520 -3395730
Locus: 12p13.33-p13.32
Gene Diseases
The TSPAN9 KRT86 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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