Gene-specific Copy Number Variation Probe-SNURF
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| Catalog: |
CNVFP-SNURF-19526 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNURF). 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: |
SNURF Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNURF genes. This product achieves the purpose of detection by hybridizing with the SNURF 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 |
SNRPN Upstream Reading Frame |
| Gene Summary [Provided by RefSeq] |
This gene is located within the Prader-Willi Syndrome critical region on chromosome 15. Transcripts produced from this gene initiate at an imprinting center and are paternally-imprinted. These transcripts may be bicistronic and also encode SNRPN (small nuclear ribonucleoprotein polypeptide N) from a downstream open reading frame. The small protein represented by this gene is encoded by an evolutionarily-conserved upstream open reading frame and is localized to the nucleus. Extensive alternative splicing and promoter usage occurs in this region and the full-length nature of some of these transcripts has not been determined. Alterations in the imprinting center are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017] |
| Gene Symbol |
SNURF |
| Location |
15q11.2 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 25200134-25223729 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-SNURF-19526-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SNURF-19526-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SNURF-19526-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SNURF-19526-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SNURF-19526-AQ |
467nm |
418nm |
|
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