Gene-specific Copy Number Variation Probe-RGR
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Catalog: |
CNVFP-RGR-17168 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RGR). 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: |
RGR Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RGR genes. This product achieves the purpose of detection by hybridizing with the RGR 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 |
Retinal G Protein Coupled Receptor |
Gene Summary [Provided by RefSeq] |
This gene encodes a putative retinal G-protein coupled receptor. The gene is a member of the opsin subfamily of the 7 transmembrane, G-protein coupled receptor 1 family. Like other opsins which bind retinaldehyde, it contains a conserved lysine residue in the seventh transmembrane domain. The protein acts as a photoisomerase to catalyze the conversion of all-trans-retinal to 11-cis-retinal. The reverse isomerization occurs with rhodopsin in retinal photoreceptor cells. The protein is exclusively expressed in tissue adjacent to retinal photoreceptor cells, the retinal pigment epithelium and Mueller cells. This gene may be associated with autosomal recessive and autosomal dominant retinitis pigmentosa (arRP and adRP, respectively). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
Gene Symbol |
RGR |
Location |
10q23.1 |
Chromosome |
Chromosome10 |
Coordinates |
This gene maps to 86004808-86018944 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-RGR-17168-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-RGR-17168-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-RGR-17168-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-RGR-17168-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-RGR-17168-AQ |
467nm |
418nm |
|
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