Gene-specific Copy Number Variation Probe-TNFSF14
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| Catalog: |
CNVFP-TNFSF14-21204 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFSF14). 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: |
TNFSF14 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFSF14 genes. This product achieves the purpose of detection by hybridizing with the TNFSF14 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 14 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF14, which is a member of the tumor necrosis factor receptor superfamily, and which is also known as a herpesvirus entry mediator (HVEM). This protein may function as a costimulatory factor for the activation of lymphoid cells and as a deterrent to infection by herpesvirus. This protein has been shown to stimulate the proliferation of T cells, and trigger apoptosis of various tumor cells. This protein is also reported to prevent tumor necrosis factor alpha mediated apoptosis in primary hepatocyte. Two alternatively spliced transcript variant encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
TNFSF14 |
| Location |
19p13.3 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 6663147-6670599 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-TNFSF14-21204-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TNFSF14-21204-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TNFSF14-21204-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TNFSF14-21204-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TNFSF14-21204-AQ |
467nm |
418nm |
|
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