Gene-specific Copy Number Variation Probe-CENPS
Add to Cart
| Catalog: |
CNVFP-CENPS-02472 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CENPS). 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: |
CENPS Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CENPS genes. This product achieves the purpose of detection by hybridizing with the CENPS 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 |
Centromere Protein S |
| Gene Summary [Provided by RefSeq] |
This gene was identified in the neuroblastoma tumor suppressor candidate region on chromosome 1p36. It contains a TFIID-31 domain, similar to that found in TATA box-binding protein-associated factor, TAF(II)31, which is required for p53-mediated transcription activation. This gene was expressed at very low levels in neuroblastoma tumors, and was shown to reduce cell growth in neuroblastoma cells, suggesting that it may have a role in a cell death pathway. The protein is a component of multiple complexes, including the Fanconi anemia (FA) core complex, the APITD1/CENPS complex, and the CENPA-CAD (nucleosome distal) complex. Known functions include an involvement with chromatin associations of the FA core complex, and a role in the stable assembly of the outer kinetochore. Alternative splicing of this gene results in multiple transcript variants. Naturally occurring read-through transcripts also exist between this gene and the downstream cortistatin (CORT) gene, as represented in GeneID:100526739. An APITD1-related pseudogene has been identified on chromosome 7. [provided by RefSeq, Nov 2010] |
| Gene Symbol |
CENPS |
| Location |
1p36.22 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 10430101-10442814 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-CENPS-02472-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CENPS-02472-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CENPS-02472-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CENPS-02472-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CENPS-02472-AQ |
467nm |
418nm |
|
Other Products
