Gene-specific Copy Number Variation Probe-NDUFV1
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| Catalog: |
CNVFP-NDUFV1-14126 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NDUFV1). 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: |
NDUFV1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NDUFV1 genes. This product achieves the purpose of detection by hybridizing with the NDUFV1 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 Core Subunit V1 |
| Gene Summary [Provided by RefSeq] |
The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinson's disease and Leigh syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009] |
| Gene Symbol |
NDUFV1 |
| Location |
11q13.2 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 67374322-67380012 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-NDUFV1-14126-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NDUFV1-14126-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NDUFV1-14126-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NDUFV1-14126-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NDUFV1-14126-AQ |
467nm |
418nm |
|
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