ENAH-LIN9 Fusion FISH Probe
The ENAH-LIN9 Fusion FISH Probe is used to confirm a fusion of the ENAH and LIN9 genes. The fusion of the ENAH and LIN9 genes has been associated with Skin Cutaneous Melanoma. 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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| ENAH-LIN9-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-RERE | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-REOR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-REGO | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-REGR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-REAQ | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-ORRE | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-OROR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-ORGO | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-ORAQ | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GORE | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GOOR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GOGO | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GOGR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GOAQ | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GRRE | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GROR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GRGO | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GRGR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-GRAQ | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-AQRE | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-AQOR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-AQGO | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-AQGR | 20 (40 μL) | 200 μL |
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| ENAH-LIN9-20-AQAQ | 20 (40 μL) | 200 μL |
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ENAH Gene Summary
This gene encodes a member of the enabled/ vasodilator-stimulated phosphoprotein. Members of this gene family are involved in actin-based motility. This protein is involved in regulating the assembly of actin filaments and modulates cell adhesion and motility. Alternate splice variants of this gene have been correlated with tumor invasiveness in certain tissues and these variants may serve as prognostic markers. A pseudogene of this gene is found on chromosome 3. [provided by RefSeq, Sep 2016]
Gene Name: ENAH, Actin Regulator
Chromosome: CHR1: 225674533 -225840845
Locus: 1q42.12
LIN9 Gene Summary
This gene encodes a tumor suppressor protein that inhibits DNA synthesis and oncogenic transformation through association with the retinoblastoma 1 protein. The encoded protein also interacts with a complex of other cell cycle regulators to repress cell cycle-dependent gene expression in non-dividing cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]
Gene Name: Lin-9 DREAM MuvB Core Complex Component
Chromosome: CHR1: 226418860 -226497198
Locus: 1q42.12
Gene Diseases
The ENAH LIN9 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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