Gene-specific Copy Number Variation Probe-AP3D1
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| Catalog: |
CNVFP-AP3D1-00913 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (AP3D1). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
AP3D1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to AP3D1 genes. This product achieves the purpose of detection by hybridizing with the AP3D1 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Adaptor Related Protein Complex 3 Delta 1 Subunit |
| Gene Summary [Provided by RefSeq] |
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 Symbol |
AP3D1 |
| Location |
19p13.3 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 2100992-2151556 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-AP3D1-00913-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-AP3D1-00913-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-AP3D1-00913-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-AP3D1-00913-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-AP3D1-00913-AQ |
467nm |
418nm |
|
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