Gene-specific Copy Number Variation Probe-TNFRSF25
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| Catalog: |
CNVFP-TNFRSF25-21216 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFRSF25). 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: |
TNFRSF25 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFRSF25 genes. This product achieves the purpose of detection by hybridizing with the TNFRSF25 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 Receptor Superfamily Member 25 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is expressed preferentially in the tissues enriched in lymphocytes, and it may play a role in regulating lymphocyte homeostasis. This receptor has been shown to stimulate NF-kappa B activity and regulate cell apoptosis. The signal transduction of this receptor is mediated by various death domain containing adaptor proteins. Knockout studies in mice suggested the role of this gene in the removal of self-reactive T cells in the thymus. Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported, most of which are potentially secreted molecules. The alternative splicing of this gene in B and T cells encounters a programmed change upon T-cell activation, which predominantly produces full-length, membrane bound isoforms, and is thought to be involved in controlling lymphocyte proliferation induced by T-cell activation. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
TNFRSF25 |
| Location |
1p36.31 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 6521213-6526255 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-TNFRSF25-21216-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TNFRSF25-21216-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TNFRSF25-21216-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TNFRSF25-21216-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TNFRSF25-21216-AQ |
467nm |
418nm |
|
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