Gene-specific Copy Number Variation Probe-NUB1
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| Catalog: |
CNVFP-NUB1-14676 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NUB1). 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: |
NUB1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NUB1 genes. This product achieves the purpose of detection by hybridizing with the NUB1 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 |
Negative Regulator Of Ubiquitin Like Proteins 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that functions as a negative regulator of NEDD8, a ubiquitin-like protein that conjugates with cullin family members in order to regulate vital biological events. The protein encoded by this gene regulates the NEDD8 conjugation system post-transcriptionally by recruiting NEDD8 and its conjugates to the proteasome for degradation. This protein interacts with the product of the AIPL1 gene, which is associated with Leber congenital amaurosis, an inherited retinopathy, and mutations in that gene can abolish interaction with this protein, which may contribute to the pathogenesis. This protein is also known to accumulate in Lewy bodies in Parkinson's disease and dementia with Lewy bodies, and in glial cytoplasmic inclusions in multiple system atrophy, with this abnormal accumulation being specific to alpha-synucleinopathy lesions. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011] |
| Gene Symbol |
NUB1 |
| Location |
7q36.1 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 151038846-151075548 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-NUB1-14676-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NUB1-14676-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NUB1-14676-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NUB1-14676-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NUB1-14676-AQ |
467nm |
418nm |
|
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