Gene-specific Copy Number Variation Probe-COX17
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| Catalog: |
CNVFP-COX17-03046 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (COX17). 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: |
COX17 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to COX17 genes. This product achieves the purpose of detection by hybridizing with the COX17 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 |
COX17, Cytochrome C Oxidase Copper Chaperone |
| Gene Summary [Provided by RefSeq] |
Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be involved in the recruitment of copper to mitochondria for incorporation into the COX apoenzyme. This protein shares 92% amino acid sequence identity with mouse and rat Cox17 proteins. This gene is no longer considered to be a candidate gene for COX deficiency. A pseudogene COX17P has been found on chromosome 13. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
COX17 |
| Location |
3q13.33 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 119388371-119396243 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-COX17-03046-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-COX17-03046-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-COX17-03046-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-COX17-03046-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-COX17-03046-AQ |
467nm |
418nm |
|
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