Gene-specific Copy Number Variation Probe-WRNIP1
Add to Cart
| Catalog: |
CNVFP-WRNIP1-22966 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WRNIP1). 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: |
WRNIP1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WRNIP1 genes. This product achieves the purpose of detection by hybridizing with the WRNIP1 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 |
Werner Helicase Interacting Protein 1 |
| Gene Summary [Provided by RefSeq] |
Werner's syndrome is a rare autosomal recessive disorder characterized by accelerated aging that is caused by defects in the Werner syndrome ATP-dependent helicase gene (WRN). The protein encoded by this gene interacts with the exonuclease-containing N-terminal portion of the Werner protein. This protein has a ubiquitin-binding zinc-finger domain in the N-terminus, an ATPase domain, and two leucine zipper motifs in the C-terminus. It has sequence similarity to replication factor C family proteins and is conserved from E. coli to human. This protein likely accumulates at sites of DNA damage by interacting with polyubiquinated proteins and also binds to DNA polymerase delta and increases the initiation frequency of DNA polymerase delta-mediated DNA synthesis. This protein also interacts with nucleoporins at nuclear pore complexes. Two transcript variants encoding different isoforms have been isolated for this gene. [provided by RefSeq, Jul 2012] |
| Gene Symbol |
WRNIP1 |
| Location |
6p25.2 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 2765665-2785979 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-WRNIP1-22966-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-WRNIP1-22966-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-WRNIP1-22966-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-WRNIP1-22966-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-WRNIP1-22966-AQ |
467nm |
418nm |
|
Other Products
