AP3D1 Break Apart FISH Probe
Empire Genomics’ AP3D1 Break Apart FISH Probe is designed to flank the AP3D1 gene and is typically used for detecting AP3D1 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.
** 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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| AP3D1BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| AP3D1BA-20-AQOR | 20 (40 μL) | 200 μL |
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| AP3D1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| AP3D1BA-20-GORE | 20 (40 μL) | 200 μL |
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| AP3D1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| AP3D1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| AP3D1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| AP3D1BA-20-REGO | 20 (40 μL) | 200 μL |
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| AP3D1BA-20-REGR | 20 (40 μL) | 200 μL |
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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 Details
Gene Symbol: AP3D1
Gene Name: Adaptor Related Protein Complex 3 Delta 1 Subunit
Chromosome: CHR19: 2100992-2151556
Locus: 19p13.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: AP3D1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: AP3D1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping