Gene-specific Copy Number Variation Probe-NMNAT1
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| Catalog: |
CNVFP-NMNAT1-14238 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NMNAT1). 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: |
NMNAT1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NMNAT1 genes. This product achieves the purpose of detection by hybridizing with the NMNAT1 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 |
Nicotinamide Nucleotide Adenylyltransferase 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes an enzyme which catalyzes a key step in the biosynthesis of nicotinamide adenine dinucleotide (NAD). The encoded enzyme is one of several nicotinamide nucleotide adenylyltransferases, and is specifically localized to the cell nucleus. Activity of this protein leads to the activation of a nuclear deacetylase that functions in the protection of damaged neurons. Mutations in this gene have been associated with Leber congenital amaurosis 9. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are located on chromosomes 1, 3, 4, 14, and 15. [provided by RefSeq, Jul 2014] |
| Gene Symbol |
NMNAT1 |
| Location |
1p36.22 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 10003485-10045556 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-NMNAT1-14238-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NMNAT1-14238-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NMNAT1-14238-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NMNAT1-14238-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NMNAT1-14238-AQ |
467nm |
418nm |
|
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