R3HDM2-KIF5A Fusion FISH Probe
The R3HDM2-KIF5A Fusion FISH Probe is used to confirm a fusion of the R3HDM2 and KIF5A genes. The fusion of the R3HDM2 and KIF5A 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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R3HDM2-KIF5A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-RERE | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-REOR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-REGO | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-REGR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-REAQ | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-ORRE | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-OROR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-ORGO | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-ORAQ | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GORE | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GOOR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GOGO | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GOGR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GOAQ | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GRRE | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GROR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GRGO | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GRGR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-GRAQ | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-AQRE | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-AQOR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-AQGO | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-AQGR | 20 (40 μL) | 200 μL | ||
R3HDM2-KIF5A-20-AQAQ | 20 (40 μL) | 200 μL |
KIF5A Gene Summary
This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10. [provided by RefSeq, Jul 2008]
Gene Name: Kinesin Family Member 5A
Chromosome: CHR12: 57943846 -57978554
Locus: 12q13.3
R3HDM2 Gene Summary
The R3H Domain Containing 2 (R3HDM2) gene is located on chr12 :57647547-57704246 at 12q13.3.
Gene Name: R3H Domain Containing 2
Chromosome: CHR12: 57647547 -57704246
Locus: 12q13.3
Gene Diseases
The R3HDM2 KIF5A 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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