Gene-specific Copy Number Variation Probe-PRPH2
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| Catalog: |
CNVFP-PRPH2-16564 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRPH2). 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: |
PRPH2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRPH2 genes. This product achieves the purpose of detection by hybridizing with the PRPH2 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 |
Peripherin 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein found in the outer segment of both rod and cone photoreceptor cells. It may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. This protein is essential for disk morphogenesis. Defects in this gene are associated with both central and peripheral retinal degenerations. Some of the various phenotypically different disorders are autosomal dominant retinitis pigmentosa, progressive macular degeneration, macular dystrophy and retinitis pigmentosa digenic. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
PRPH2 |
| Location |
6p21.1 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 42664332-42690358 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-PRPH2-16564-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PRPH2-16564-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PRPH2-16564-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PRPH2-16564-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PRPH2-16564-AQ |
467nm |
418nm |
|
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