Gene-specific Copy Number Variation Probe-DDX39B
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| Catalog: |
CNVFP-DDX39B-03836 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DDX39B). 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: |
DDX39B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DDX39B genes. This product achieves the purpose of detection by hybridizing with the DDX39B 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 39B |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011] |
| Gene Symbol |
DDX39B |
| Location |
6p21.33 |
| Chromosome |
Chromosome6_ssto_hap7 |
| Coordinates |
This gene maps to 2828800-2841057 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-DDX39B-03836-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DDX39B-03836-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DDX39B-03836-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DDX39B-03836-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DDX39B-03836-AQ |
467nm |
418nm |
|
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