Gene-specific Copy Number Variation Probe-NUS1
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| Catalog: |
CNVFP-NUS1-14633 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NUS1). 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: |
NUS1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NUS1 genes. This product achieves the purpose of detection by hybridizing with the NUS1 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 |
NUS1 Dehydrodolichyl Diphosphate Synthase Subunit |
| Gene Summary [Provided by RefSeq] |
This gene encodes a type I single transmembrane domain receptor, which is a subunit of cis-prenyltransferase, and serves as a specific receptor for the neural and cardiovascular regulator Nogo-B. The encoded protein is essential for dolichol synthesis and protein glycosylation. This gene is highly expressed in non-small cell lung carcinomas as well as estrogen receptor-alpha positive breast cancer cells where it promotes epithelial mesenchymal transition. This gene is associated with the poor prognosis of human hepatocellular carcinoma patients. Naturally occurring mutations in this gene cause a congenital disorder of glycosylation and are associated with epilepsy. A knockout of the orthologous gene in mice causes embryonic lethality before day 6.5. Pseudogenes of this gene have been defined on chromosomes 13 and X. [provided by RefSeq, May 2017] |
| Gene Symbol |
NUS1 |
| Location |
6q22.1 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 117996616-118031886 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-NUS1-14633-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NUS1-14633-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NUS1-14633-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NUS1-14633-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NUS1-14633-AQ |
467nm |
418nm |
|
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