Gene-specific Copy Number Variation Probe-NYX
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| Catalog: |
CNVFP-NYX-14585 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NYX). 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: |
NYX Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NYX genes. This product achieves the purpose of detection by hybridizing with the NYX 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 |
Nyctalopin |
| Gene Summary [Provided by RefSeq] |
The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB. [provided by RefSeq, Oct 2008] |
| Gene Symbol |
NYX |
| Location |
Xp11.4 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 41306712-41334905 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-NYX-14585-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NYX-14585-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NYX-14585-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NYX-14585-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NYX-14585-AQ |
467nm |
418nm |
|
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