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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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
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
Brain Lower Grade Glioma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.