Gene-specific Copy Number Variation Probe-TNFRSF10C
Add to Cart
Catalog: |
CNVFP-TNFRSF10C-21226 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFRSF10C). 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: |
TNFRSF10C Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFRSF10C genes. This product achieves the purpose of detection by hybridizing with the TNFRSF10C 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 10c |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain and a transmembrane domain, but no cytoplasmic death domain. This receptor is not capable of inducing apoptosis, and is thought to function as an antagonistic receptor that protects cells from TRAIL-induced apoptosis. This gene was found to be a p53-regulated DNA damage-inducible gene. The expression of this gene was detected in many normal tissues but not in most cancer cell lines, which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL. [provided by RefSeq, Jul 2008] |
Gene Symbol |
TNFRSF10C |
Location |
8p21.3 |
Chromosome |
Chromosome8 |
Coordinates |
This gene maps to 22960326-22974950 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-TNFRSF10C-21226-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-TNFRSF10C-21226-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-TNFRSF10C-21226-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-TNFRSF10C-21226-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-TNFRSF10C-21226-AQ |
467nm |
418nm |
|
Other Products