Gene-specific Copy Number Variation Probe-NUP214
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| Catalog: |
CNVFP-NUP214-14649 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NUP214). 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: |
NUP214 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NUP214 genes. This product achieves the purpose of detection by hybridizing with the NUP214 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 |
Nucleoporin 214 |
| Gene Summary [Provided by RefSeq] |
The nuclear pore complex is a massive structure that extends across the nuclear envelope, forming a gateway that regulates the flow of macromolecules between the nucleus and the cytoplasm. Nucleoporins are the main components of the nuclear pore complex in eukaryotic cells. This gene is a member of the FG-repeat-containing nucleoporins. The protein encoded by this gene is localized to the cytoplasmic face of the nuclear pore complex where it is required for proper cell cycle progression and nucleocytoplasmic transport. The 3' portion of this gene forms a fusion gene with the DEK gene on chromosome 6 in a t(6,9) translocation associated with acute myeloid leukemia and myelodysplastic syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015] |
| Gene Symbol |
NUP214 |
| Location |
9q34.13 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 134000980-134109091 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-NUP214-14649-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NUP214-14649-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NUP214-14649-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NUP214-14649-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NUP214-14649-AQ |
467nm |
418nm |
|
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