Gene-specific Copy Number Variation Probe-CEP78
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| Catalog: |
CNVFP-CEP78-02397 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CEP78). 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: |
CEP78 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CEP78 genes. This product achieves the purpose of detection by hybridizing with the CEP78 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 |
Centrosomal Protein 78 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a centrosomal protein that is both required for the regulation of centrosome-related events during the cell cycle, and required for ciliogenesis. The encoded protein has an N-terminal leucine-rich repeat (LRR) domain with six consecutive LRR repeats, and a C-terminal coiled-coil domain. It interacts with the N-terminal catalytic domain of polo-like kinase 4 (PLK4) and colocalizes with PLK4 to the distal end of the centriole. Naturally occurring mutations in this gene cause defects in primary cilia that result in retinal degeneration and sensorineural hearing loss which are associated with cone-rod degeneration disease as well as Usher syndrome. Low expression of this gene is associated with poor prognosis of colorectal cancer patients. [provided by RefSeq, Mar 2017] |
| Gene Symbol |
CEP78 |
| Location |
9q21.2 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 80850990-80881983 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-CEP78-02397-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CEP78-02397-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CEP78-02397-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CEP78-02397-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CEP78-02397-AQ |
467nm |
418nm |
|
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