Gene-specific Copy Number Variation Probe-NBR1
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| Catalog: |
CNVFP-NBR1-13871 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NBR1). 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: |
NBR1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NBR1 genes. This product achieves the purpose of detection by hybridizing with the NBR1 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 |
NBR1, Autophagy Cargo Receptor |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene was originally identified as an ovarian tumor antigen monitored in ovarian cancer. The encoded protein contains a B-box/coiled-coil motif, which is present in many genes with transformation potential. It functions as a specific autophagy receptor for the selective autophagic degradation of peroxisomes by forming intracellular inclusions with ubiquitylated autophagic substrates. This gene is located on a region of chromosome 17q21.1 that is in close proximity to the BRCA1 tumor suppressor gene. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2014] |
| Gene Symbol |
NBR1 |
| Location |
17q21.31 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 41322497-41363707 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-NBR1-13871-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NBR1-13871-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NBR1-13871-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NBR1-13871-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NBR1-13871-AQ |
467nm |
418nm |
|
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