Gene-specific Copy Number Variation Probe-NDUFB9
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| Catalog: |
CNVFP-NDUFB9-14139 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NDUFB9). 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: |
NDUFB9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NDUFB9 genes. This product achieves the purpose of detection by hybridizing with the NDUFB9 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 |
NADH:ubiquinone Oxidoreductase Subunit B9 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015] |
| Gene Symbol |
NDUFB9 |
| Location |
8q24.13 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 125551342-125562227 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-NDUFB9-14139-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NDUFB9-14139-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NDUFB9-14139-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NDUFB9-14139-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NDUFB9-14139-AQ |
467nm |
418nm |
|
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