Gene-specific Copy Number Variation Probe-TNFSF8
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| Catalog: |
CNVFP-TNFSF8-21123 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFSF8). 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: |
TNFSF8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFSF8 genes. This product achieves the purpose of detection by hybridizing with the TNFSF8 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 |
TNF Superfamily Member 8 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This cytokine is a ligand for TNFRSF8/CD30, which is a cell surface antigen and a marker for Hodgkin lymphoma and related hematologic malignancies. The engagement of this cytokine expressed on B cell surface plays an inhibitory role in modulating Ig class switch. This cytokine was shown to enhance cell proliferation of some lymphoma cell lines, while to induce cell death and reduce cell proliferation of other lymphoma cell lines. The pleiotropic biologic activities of this cytokine on different CD30+ lymphoma cell lines may play a pathophysiologic role in Hodgkin's and some non-Hodgkin's lymphomas. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011] |
| Gene Symbol |
TNFSF8 |
| Location |
9q32-q33.1 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 117665123-117692770 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-TNFSF8-21123-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TNFSF8-21123-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TNFSF8-21123-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TNFSF8-21123-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TNFSF8-21123-AQ |
467nm |
418nm |
|
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