Gene-specific Copy Number Variation Probe-TNFSF13
Add to Cart
| Catalog: |
CNVFP-TNFSF13-21205 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFSF13). 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: |
TNFSF13 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFSF13 genes. This product achieves the purpose of detection by hybridizing with the TNFSF13 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 13 |
| 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 TNFRSF17/BCMA, a member of the TNF receptor family. This protein and its receptor are both found to be important for B cell development. In vitro experiments suggested that this protein may be able to induce apoptosis through its interaction with other TNF receptor family proteins such as TNFRSF6/FAS and TNFRSF14/HVEM. Alternative splicing results in multiple transcript variants. Some transcripts that skip the last exon of the upstream gene (TNFSF12) and continue into the second exon of this gene have been identified; such read-through transcripts are contained in GeneID 407977, TNFSF12-TNFSF13. [provided by RefSeq, Oct 2010] |
| Gene Symbol |
TNFSF13 |
| Location |
17p13.1 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 7461608-7464925 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-TNFSF13-21205-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TNFSF13-21205-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TNFSF13-21205-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TNFSF13-21205-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TNFSF13-21205-AQ |
467nm |
418nm |
|
Other Products
