Gene-specific Copy Number Variation Probe-RNF170
Add to Cart
| Catalog: |
CNVFP-RNF170-17659 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RNF170). 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: |
RNF170 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RNF170 genes. This product achieves the purpose of detection by hybridizing with the RNF170 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 |
Ring Finger Protein 170 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a RING domain-containing protein that resides in the endoplasmic reticulum (ER) membrane. This protein functions as an E3 ubiquitin ligase and mediates ubiquitination and processing of inositol 1,4,5-trisphosphate (IP3) receptors via the ER-associated protein degradation pathway. It is recruited to the activated IP3 receptors by the ERLIN1/ERLIN2 complex to which it is constitutively bound. Mutations in this gene are associated with autosomal dominant sensory ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012] |
| Gene Symbol |
RNF170 |
| Location |
8p11.21 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 42704779-42751866 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-RNF170-17659-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RNF170-17659-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RNF170-17659-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RNF170-17659-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RNF170-17659-AQ |
467nm |
418nm |
|
Other Products
