Gene-specific Copy Number Variation Probe-DDX39A
Add to Cart
| Catalog: |
CNVFP-DDX39A-03834 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DDX39A). 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: |
DDX39A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DDX39A genes. This product achieves the purpose of detection by hybridizing with the DDX39A 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 |
DExD-box Helicase 39A |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the DEAD box protein family. These proteins are characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD) and are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene is thought to play a role in the prognosis of patients with gastrointestinal stromal tumors. A pseudogene of this gene is present on chromosome 13. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Sep 2013] |
| Gene Symbol |
DDX39A |
| Location |
19p13.12 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 14519609-14530195 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-DDX39A-03834-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DDX39A-03834-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DDX39A-03834-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DDX39A-03834-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DDX39A-03834-AQ |
467nm |
418nm |
|
Other Products
