Gene-specific Copy Number Variation Probe-AIPL1
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| Catalog: |
CNVFP-AIPL1-00338 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (AIPL1). 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: |
AIPL1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to AIPL1 genes. This product achieves the purpose of detection by hybridizing with the AIPL1 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 |
Aryl Hydrocarbon Receptor Interacting Protein Like 1 |
| Gene Summary [Provided by RefSeq] |
Leber congenital amaurosis (LCA) is the most severe inherited retinopathy with the earliest age of onset and accounts for at least 5% of all inherited retinal diseases. Affected individuals are diagnosed at birth or in the first few months of life with nystagmus, severely impaired vision or blindness and an abnormal or flat electroretinogram. The photoreceptor/pineal-expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, is located within the LCA4 candidate region. The encoded protein contains three tetratricopeptide motifs, consistent with chaperone or nuclear transport activity. Mutations in this gene may cause approximately 20% of recessive LCA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014] |
| Gene Symbol |
AIPL1 |
| Location |
17p13.2 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 6327058-6338519 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-AIPL1-00338-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-AIPL1-00338-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-AIPL1-00338-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-AIPL1-00338-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-AIPL1-00338-AQ |
467nm |
418nm |
|
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