Gene-specific Copy Number Variation Probe-OPN1MW2
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| Catalog: |
CNVFP-OPN1MW2-14526 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (OPN1MW2). 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: |
OPN1MW2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to OPN1MW2 genes. This product achieves the purpose of detection by hybridizing with the OPN1MW2 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 |
Opsin 1, Medium Wave Sensitive 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness. [provided by RefSeq, Mar 2009] |
| Gene Symbol |
OPN1MW2 |
| Location |
Xq28 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 153485202-153498755 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-OPN1MW2-14526-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-OPN1MW2-14526-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-OPN1MW2-14526-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-OPN1MW2-14526-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-OPN1MW2-14526-AQ |
467nm |
418nm |
|
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