Gene-specific Copy Number Variation Probe-RASD2
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Catalog: |
CNVFP-RASD2-17044 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RASD2). 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: |
RASD2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RASD2 genes. This product achieves the purpose of detection by hybridizing with the RASD2 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 |
RASD Family Member 2 |
Gene Summary [Provided by RefSeq] |
This gene belongs to the Ras superfamily of small GTPases and is enriched in the striatum. The encoded protein functions as an E3 ligase for attachment of small ubiquitin-like modifier (SUMO). This protein also binds to mutant huntingtin (mHtt), the protein mutated in Huntington disease (HD). Sumoylation of mHTT by this protein may cause degeneration of the striatum. The protein functions as an activator of mechanistic target of rapamycin 1 (mTOR1), which in turn plays a role in myelination, axon growth and regeneration. Reduced levels of mRNA expressed by this gene were found in HD patients. [provided by RefSeq, Jan 2016] |
Gene Symbol |
RASD2 |
Location |
22q12.3 |
Chromosome |
Chromosome22 |
Coordinates |
This gene maps to 35937351-35950045 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-RASD2-17044-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-RASD2-17044-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-RASD2-17044-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-RASD2-17044-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-RASD2-17044-AQ |
467nm |
418nm |
|
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