Gene-specific Copy Number Variation Probe-NOL8
Add to Cart
Catalog: |
CNVFP-NOL8-14206 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NOL8). 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: |
NOL8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NOL8 genes. This product achieves the purpose of detection by hybridizing with the NOL8 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 |
Nucleolar Protein 8 |
Gene Summary [Provided by RefSeq] |
NOL8 binds Ras-related GTP-binding proteins (see MIM 608267) and plays a role in cell growth (Sekiguchi et al., 2004 [PubMed 14660641]).[supplied by OMIM, Mar 2008] |
Gene Symbol |
NOL8 |
Location |
9q22.31 |
Chromosome |
Chromosome9 |
Coordinates |
This gene maps to 95059639-95087876 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-NOL8-14206-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-NOL8-14206-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-NOL8-14206-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-NOL8-14206-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-NOL8-14206-AQ |
467nm |
418nm |
|
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