Gene-specific Copy Number Variation Probe-PWRN1
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| Catalog: |
CNVFP-PWRN1-16941 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PWRN1). 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: |
PWRN1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PWRN1 genes. This product achieves the purpose of detection by hybridizing with the PWRN1 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 |
Prader-Willi Region Non-protein Coding RNA 1 |
| Gene Summary [Provided by RefSeq] |
This gene is located in the Prader-Willi syndrome (PWS) region of chromosome 15, which is known to undergo imprinting. The transcript is believed to be non-coding. It is bi-allelically expressed in testis and kidney, but mono-allelically expressed from the paternal allele in brain. This gene is poly-adenylated and is known to undergo alternative splicing. Transcript variants may represent part of a complex imprinting center-SNURF-SNRPN transcription unit. The contribution of this gene to the PWS phenotype is unknown, but it has been suggested that it may play a role in establishing paternal imprinting in the PWS region, perhaps by maintaining the paternal allele in an open chromatin configuration. [provided by RefSeq, Sep 2009] |
| Gene Symbol |
PWRN1 |
| Location |
15q11.2 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 24803303-24832926 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-PWRN1-16941-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PWRN1-16941-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PWRN1-16941-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PWRN1-16941-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PWRN1-16941-AQ |
467nm |
418nm |
|
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