LRRC16A-DCDC2 Fusion FISH Probe
The LRRC16A-DCDC2 Fusion FISH Probe is used to confirm a fusion of the LRRC16A and DCDC2 genes. The fusion of the LRRC16A and DCDC2 genes has been associated with Mesothelioma. 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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| LRRC16A-DCDC2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-RERE | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-REOR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-REGO | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-REGR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-REAQ | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-ORRE | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-OROR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-ORGO | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-ORAQ | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GORE | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GOOR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GOGO | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GOGR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GOAQ | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GRRE | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GROR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GRGO | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GRGR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-GRAQ | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-AQRE | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-AQOR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-AQGO | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-AQGR | 20 (40 μL) | 200 μL |
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| LRRC16A-DCDC2-20-AQAQ | 20 (40 μL) | 200 μL |
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DCDC2 Gene Summary
This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2013]
Gene Name: Doublecortin Domain Containing 2
Chromosome: CHR6: 24171982 -24383520
Locus: 6p22.3
Gene Diseases
The LRRC16A DCDC2 Fusion has been associated with the following diseases:
| Disease Name |
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| Mesothelioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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