Gene-specific Copy Number Variation Probe-TNFSF12
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| Catalog: |
CNVFP-TNFSF12-21208 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFSF12). 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: |
TNFSF12 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFSF12 genes. This product achieves the purpose of detection by hybridizing with the TNFSF12 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 12 |
| 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 protein is a ligand for the FN14/TWEAKR receptor. This cytokine has overlapping signaling functions with TNF, but displays a much wider tissue distribution. This cytokine, which exists in both membrane-bound and secreted forms, can induce apoptosis via multiple pathways of cell death in a cell type-specific manner. This cytokine is also found to promote proliferation and migration of endothelial cells, and thus acts as a regulator of angiogenesis. Alternative splicing results in multiple transcript variants. Some transcripts skip the last exon of this gene and continue into the second exon of the neighboring TNFSF13 gene; such read-through transcripts are contained in GeneID 407977, TNFSF12-TNFSF13. [provided by RefSeq, Oct 2010] |
| Gene Symbol |
TNFSF12 |
| Location |
17p13.1 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 7452374-7461207 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-TNFSF12-21208-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TNFSF12-21208-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TNFSF12-21208-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TNFSF12-21208-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TNFSF12-21208-AQ |
467nm |
418nm |
|
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