APOL2-ULK2 Fusion FISH Probe
The APOL2-ULK2 Fusion FISH Probe is used to confirm a fusion of the APOL2 and ULK2 genes. The fusion of the APOL2 and ULK2 genes has been associated with Lung Squamous Cell Carcinoma. 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| APOL2-ULK2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-RERE | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-REOR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-REGO | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-REGR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-REAQ | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-ORRE | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-OROR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-ORGO | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-ORAQ | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GORE | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GOOR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GOGO | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GOGR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GOAQ | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GRRE | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GROR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GRGO | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GRGR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-GRAQ | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-AQRE | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-AQOR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-AQGO | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-AQGR | 20 (40 μL) | 200 μL |
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| APOL2-ULK2-20-AQAQ | 20 (40 μL) | 200 μL |
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ULK2 Gene Summary
This gene encodes a protein that is similar to a serine/threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2008]
Gene Name: Unc-51 Like Autophagy Activating Kinase 2
Chromosome: CHR17: 19674142 -19771239
Locus: 17p11.2
APOL2 Gene Summary
This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Apolipoprotein L2
Chromosome: CHR22: 36622254 -36636000
Locus: 22q12.3
Gene Diseases
The APOL2 ULK2 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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