Gene-specific Copy Number Variation Probe-PSPC1
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| Catalog: |
CNVFP-PSPC1-16750 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PSPC1). 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: |
PSPC1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PSPC1 genes. This product achieves the purpose of detection by hybridizing with the PSPC1 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 |
Paraspeckle Component 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a nucleolar protein that localizes to punctate subnuclear structures that occur close to splicing speckles, known as paraspeckles. These paraspeckles are composed of RNA-protein structures that include a non-coding RNA, NEAT1/Men epsilon/beta, and the Drosophila Behavior Human Splicing family of proteins, which include the product of this gene and the P54NRB/NONO and PSF/SFPQ proteins. Paraspeckles may function in the control of gene expression via an RNA nuclear retention mechanism. The protein encoded by this gene is found in paraspeckles in transcriptionally active cells, but it localizes to unique cap structures at the nucleolar periphery when RNA polymerase II transcription is inhibited, or during telophase. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene, which is also located on chromosome 13, has been identified. [provided by RefSeq, Aug 2011] |
| Gene Symbol |
PSPC1 |
| Location |
13q12.11 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 20248891-20357159 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-PSPC1-16750-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PSPC1-16750-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PSPC1-16750-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PSPC1-16750-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PSPC1-16750-AQ |
467nm |
418nm |
|
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