Gene-specific Copy Number Variation Probe-RP1
Add to Cart
| Catalog: |
CNVFP-RP1-17588 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RP1). 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: |
RP1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RP1 genes. This product achieves the purpose of detection by hybridizing with the RP1 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 |
RP1, Axonemal Microtubule Associated |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains, which bind microtubules and regulate microtubule polymerization. The encoded protein is a photoreceptor microtubule-associated protein and is required for correct stacking of outer segment disc. This protein and the RP1L1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Because of its response to in vivo retinal oxygen levels, this protein was initially named ORP1 (oxygen-regulated protein-1). This protein was subsequently designated RP1 (retinitis pigmentosa 1) when it was found that mutations in this gene cause autosomal dominant retinitis pigmentosa. Mutations in this gene also cause autosomal recessive retinitis pigmentosa. Transcript variants resulted from an alternative promoter and alternative splicings have been found, which overlap the current reference sequence and has several exons upstream and downstream of the current reference sequence. However, the biological validity and full-length nature of some variants cannot be determined at this time.[provided by RefSeq, Sep 2010] |
| Gene Symbol |
RP1 |
| Location |
8q11.23-q12.1 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 55528626-55543394 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-RP1-17588-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RP1-17588-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RP1-17588-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RP1-17588-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RP1-17588-AQ |
467nm |
418nm |
|
Other Products
