AP3D1-KCTD19 Fusion FISH Probe
The AP3D1-KCTD19 Fusion FISH Probe is used to confirm a fusion of the AP3D1 and KCTD19 genes. The fusion of the AP3D1 and KCTD19 genes has been associated with Prostate Adenocarcinoma. 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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| AP3D1-KCTD19-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-RERE | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-REOR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-REGO | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-REGR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-REAQ | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-ORRE | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-OROR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-ORGO | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-ORAQ | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GORE | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GOOR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GOGO | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GOGR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GOAQ | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GRRE | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GROR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GRGO | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GRGR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-GRAQ | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-AQRE | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-AQOR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-AQGO | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-AQGR | 20 (40 μL) | 200 μL |
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| AP3D1-KCTD19-20-AQAQ | 20 (40 μL) | 200 μL |
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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
KCTD19 Gene Summary
The Potassium Channel Tetramerization Domain Containing 19 (KCTD19) gene is located on chr16 :67323392-67360661 at 16q22.1.
Gene Name: Potassium Channel Tetramerization Domain Containing 19
Chromosome: CHR16: 67323392 -67360661
Locus: 16q22.1
Gene Diseases
The AP3D1 KCTD19 Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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