Gene-specific Copy Number Variation Probe-NDUFS7
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| Catalog: |
CNVFP-NDUFS7-14128 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NDUFS7). 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: |
NDUFS7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NDUFS7 genes. This product achieves the purpose of detection by hybridizing with the NDUFS7 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 S7 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
NDUFS7 |
| Location |
19p13.3 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 1383882-1395588 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-NDUFS7-14128-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NDUFS7-14128-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NDUFS7-14128-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NDUFS7-14128-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NDUFS7-14128-AQ |
467nm |
418nm |
|
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