Gene-specific Copy Number Variation Probe-TNFRSF11A
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| Catalog: |
CNVFP-TNFRSF11A-21225 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFRSF11A). 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: |
TNFRSF11A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFRSF11A genes. This product achieves the purpose of detection by hybridizing with the TNFRSF11A 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 11a |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptors can interact with various TRAF family proteins, through which this receptor induces the activation of NF-kappa B and MAPK8/JNK. This receptor and its ligand are important regulators of the interaction between T cells and dendritic cells. This receptor is also an essential mediator for osteoclast and lymph node development. Mutations at this locus have been associated with familial expansile osteolysis, autosomal recessive osteopetrosis, and Paget disease of bone. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Aug 2012] |
| Gene Symbol |
TNFRSF11A |
| Location |
18q21.33 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 59992547-60053504 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-TNFRSF11A-21225-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TNFRSF11A-21225-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TNFRSF11A-21225-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TNFRSF11A-21225-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TNFRSF11A-21225-AQ |
467nm |
418nm |
|
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