Gene-specific Copy Number Variation Probe-RP1L1
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| Catalog: |
CNVFP-RP1L1-17587 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RP1L1). 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: |
RP1L1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RP1L1 genes. This product achieves the purpose of detection by hybridizing with the RP1L1 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 Like 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, and two C-terminal large repetitive regions, both of which contain a high percentage of glutamine and glutamic acid residues. This protein is a retinal-specific protein. Its exact length varies among individuals due to the presence of a 16aa repeat in the first C-terminal repetitive region. The 16aa repeat is encoded by the highly polymorphic 48-bp repeat, and 1-6 copies of the 16aa repeat have been identified in normal individuals. The current reference sequence shown here has a single copy of the 16aa repeat. This protein and the RP1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Mutations in this gene cause occult macular dystrophy (OMD). [provided by RefSeq, Sep 2010] |
| Gene Symbol |
RP1L1 |
| Location |
8p23.1 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 10463859-10512617 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-RP1L1-17587-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RP1L1-17587-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RP1L1-17587-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RP1L1-17587-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RP1L1-17587-AQ |
467nm |
418nm |
|
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