TBC1D22A-AP3D1 Fusion FISH Probe
The TBC1D22A-AP3D1 Fusion FISH Probe is used to confirm a fusion of the TBC1D22A and AP3D1 genes. The fusion of the TBC1D22A and AP3D1 genes has been associated with Uterine Carcinosarcoma. 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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| TBC1D22A-AP3D1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-RERE | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-REOR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-REGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-REGR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-REAQ | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-ORRE | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-OROR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-ORGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-ORAQ | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GORE | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GOOR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GOGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GOGR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GOAQ | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GRRE | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GROR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GRGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GRGR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-GRAQ | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-AQRE | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-AQOR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-AQGO | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-AQGR | 20 (40 μL) | 200 μL |
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| TBC1D22A-AP3D1-20-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
TBC1D22A Gene Summary
The TBC1 Domain Family Member 22A (TBC1D22A) gene is located on chr22 :47158517-47571342 at 22q13.31.
Gene Name: TBC1 Domain Family Member 22A
Chromosome: CHR22: 47158517 -47571342
Locus: 22q13.31
Gene Diseases
The TBC1D22A AP3D1 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Carcinosarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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