Gene-specific Copy Number Variation Probe-SNRPN
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Catalog: |
CNVFP-SNRPN-19498 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNRPN). 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: |
SNRPN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNRPN genes. This product achieves the purpose of detection by hybridizing with the SNRPN 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 |
Small Nuclear Ribonucleoprotein Polypeptide N |
Gene Summary [Provided by RefSeq] |
This gene is located within the Prader-Willi Syndrome critical region on chromosome 15 and is imprinted and expressed from the paternal allele. It encodes a component of the small nuclear ribonucleoprotein complex, which functions in pre-mRNA processing and may contribute to tissue-specific alternative splicing. Alternative promoter use and alternative splicing result in a multitude of transcript variants encoding the same protein. Transcript variants that initiate at the CpG island-associated imprinting center may be bicistronic and also encode the SNRPN upstream reading frame protein (SNURF) from an upstream open reading frame. In addition, long spliced transcripts for small nucleolar RNA host gene 14 (SNHG14) may originate from the promoters at this locus and share exons with this gene. Alterations in this region are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017] |
Gene Symbol |
SNRPN |
Location |
15q11.2 |
Chromosome |
Chromosome15 |
Coordinates |
This gene maps to 25068793-25223729 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-SNRPN-19498-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SNRPN-19498-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SNRPN-19498-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SNRPN-19498-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SNRPN-19498-AQ |
467nm |
418nm |
|
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