ZNF69-AP3D1 Fusion FISH Probe
The ZNF69-AP3D1 Fusion FISH Probe is used to confirm a fusion of the ZNF69 and AP3D1 genes. The fusion of the ZNF69 and AP3D1 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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| ZNF69-AP3D1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-RERE | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-REOR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-REGO | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-REGR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-REAQ | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-ORRE | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-OROR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-ORGO | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-ORAQ | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GORE | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GOOR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GOGO | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GOGR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GOAQ | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GRRE | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GROR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GRGO | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GRGR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-GRAQ | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-AQRE | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-AQOR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-AQGO | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-AQGR | 20 (40 μL) | 200 μL |
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| ZNF69-AP3D1-20-AQAQ | 20 (40 μL) | 200 μL |
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ZNF69 Gene Summary
The Zinc Finger Protein 69 (ZNF69) gene is located on chr19 :11998669-12025365 at 19p13.2.
Gene Name: Zinc Finger Protein 69
Chromosome: CHR19: 11998669 -12025365
Locus: 19p13.2
AP3D1 Gene Summary
The protein encoded by this gene is a subunit of the AP3 adaptor-like complex, which is not clathrin-associated, but is associated with the golgi region, as well as more peripheral structures. The AP-3 complex facilitates the budding of vesicles from the golgi membrane, and may be directly involved in trafficking to lysosomes. This subunit is implicated in intracellular biogenesis and trafficking of pigment granules, and possibly platelet dense granules and neurotransmitter vesicles. Defects in this gene are a cause of a new type of Hermansky-Pudlak syndrome. [provided by RefSeq, Feb 2017]
Gene Name: Adaptor Related Protein Complex 3 Delta 1 Subunit
Chromosome: CHR19: 2100992 -2151556
Locus: 19p13.3
Gene Diseases
The ZNF69 AP3D1 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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