Gene-specific Copy Number Variation Probe-RNF213
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| Catalog: |
CNVFP-RNF213-17642 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RNF213). 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: |
RNF213 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RNF213 genes. This product achieves the purpose of detection by hybridizing with the RNF213 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 213 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein containing a C3HC4-type RING finger domain, which is a specialized type of Zn-finger that binds two atoms of zinc and is thought to be involved in mediating protein-protein interactions. The protein also contains an AAA domain, which is associated with ATPase activity. This gene is a susceptibility gene for Moyamoya disease, a vascular disorder of intracranial arteries. This gene is also a translocation partner in anaplastic large cell lymphoma and inflammatory myofibroblastic tumor cases, where a t(2;17)(p23;q25) translocation has been identified with the anaplastic lymphoma kinase (ALK) gene on chromosome 2, and a t(8;17)(q24;q25) translocation has been identified with the MYC gene on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011] |
| Gene Symbol |
RNF213 |
| Location |
17q25.3 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 78234666-78370086 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-RNF213-17642-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RNF213-17642-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RNF213-17642-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RNF213-17642-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RNF213-17642-AQ |
467nm |
418nm |
|
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